Acetaminophen

Synopsis, Chemistry

APIs // Active Pharmaceutical Ingredients

118 API Suppliers, 84 USDMF, 20 CEP/COS, 16 JDMF, 7 EU WC, 108 KDMF, 105 NDC API, 28 Listed Suppliers

DEVELOPMENTS

36 Drug(s) in Development

36 Drug(s) in Development

PRICE INFORMATION

API Reference Price, API Exports, API Imports, FDF Exports, FDF Imports

DOSSIERs // Finished Dosage Formulations

2413 Dossiers, 727 FDA Orange Book, 482 Europe, 299 Canada, 73 Australia, 376 South Africa, 456 Listed Dossiers

DRUG PRODUCT COMPOSITION

SUPPOSITORY;RECTAL - 120MG, SUPPOSITORY;RECTAL - 325MG, SUPPOSITORY;RECTAL - 650MG, SUPPOSITORY;RECTAL - 80MG, CAPSULE;ORAL - 325MG;50MG;40MG;30MG, TABLET, EXTENDED RELEASE;ORAL - 325MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - 250MG;250MG;65MG, TABLET;ORAL - 325MG;37.5MG, SOLUTION;INTRAVENOUS - 1GM/100ML (10MG/ML), TABLET;ORAL - 300MG;15MG, TABLET;ORAL - 300MG;30MG, TABLET;ORAL - 300MG;60MG, TABLET;ORAL - 325MG;5MG, TABLET;ORAL - 325MG;50MG;40MG, TABLET;ORAL - 300MG;60MG

SUPPOSITORY;RECTAL - 120MG
SUPPOSITORY;RECTAL - 325MG
SUPPOSITORY;RECTAL - 650MG
SUPPOSITORY;RECTAL - 80MG
CAPSULE;ORAL - 325MG;50MG;40MG;30MG
TABLET, EXTENDED RELEASE;ORAL - 325MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - 250MG;250MG;65MG
TABLET;ORAL - 325MG;37.5MG
SOLUTION;INTRAVENOUS - 1GM/100ML (10MG/ML)
TABLET;ORAL - 300MG;15MG
TABLET;ORAL - 300MG;30MG
TABLET;ORAL - 300MG;60MG
TABLET;ORAL - 325MG;5MG
TABLET;ORAL - 325MG;50MG;40MG
TABLET;ORAL - 300MG;60MG

RELATED EXCIPIENT COMPANIES

Suppliers, 56 Roquette, 44 BASF, 39 Kerry, 31 SPI Pharma, 27 Microlex e.U, 22 Seppic, 22 Nanjing Well Pharmaceutical, 19 Actylis, 17 Gangwal Chemicals, 16 Gangwal Healthcare, 14 Rochem International Inc, 13 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd, 12 Sigachi Industries, 12 Corel Pharma Chem, 12 Boai NKY Pharmaceuticals Ltd, 8 Shanghai Shenmei Pharmaceutical Technology Co., Ltd, 8 DKSH, 8 Beneo, 7 DFE Pharma, 7 Ideal Cures Pvt Ltd, 6 Lonza Capsugel, 6 Clariant, 5 Kima Chemical, 5 Vasa Pharmachem, 5 Ingredion Pharma Solutions, 5 Prachin Chemical, 5 Pharmatrans-Sanaq, 4 Ulanqab Kema New Material, 4 Finar, 4 ACG Worldwide, 4 Alcedo Pharmachem, 4 The Dow Chemical Company, 3 Shijiazhuang Huaxu Pharmaceutical, 3 Aeon Procare, 3 Pharm-RX Chemical, 3 Jai Radhe Sales, 3 Zhejiang Huakang Pharmaceutical, 2 Seqens, 2 Bioplus Life Sciences, 2 Huzhou Sunflower Pharmaceutical, 2 Pfanstiehl, 2 Nanjing Bold Chemical, 2 Nomisma Healthcare, 2 Qualicaps, 2 Minakem, 1 Qianhao Chemical (Hebei) Co., Ltd, 1 Evonik, 1 Shanghai Welltone Material Technology Co., Ltd, 1 NEWEDGE Overseas, 1 Chynops Pharma, 1 Avesta Pharma

EXCIPIENTS BY APPLICATIONS

126 Fillers, Diluents & Binders, 67 Solubilizers, 67 Coating Systems & Additives, 61 Thickeners and Stabilizers, 59 Taste Masking, 56 Direct Compression, 50 Disintegrants & Superdisintegrants, 48 Topical, 44 Parenteral, 40 Controlled & Modified Release, 39 Granulation, 39 Lubricants & Glidants, 38 Film Formers & Plasticizers, 27 Chewable & Orodispersible Aids, 20 Co-Processed Excipients, 20 Emulsifying Agents, 13 API Stability Enhancers, 12 Surfactant & Foaming Agents, 9 Empty Capsules, 9 Rheology Modifiers, 4 Vegetarian Capsules, 2 Coloring Agents, 1 Soft Gelatin

GLOBAL SALES INFORMATION

32 US Medicaid Prescriptions, 381 Finished Drug Prices

MARKET PLACE

164 APIs, 93 DOSSIERS // FDF

PATENTS

40 US Patents, 1 US Exclusivities, 3 Health Canada Patents

ANALYTICAL SOLUTION(s)

2 BioAnalytical Methods, 8 Analytical Solutions, 1 EDQM Standards, 7 USP Standards, 1 JP Standards, 21 Other Ref. Standards

DIGITAL CONTENT

10 Data Compilations & Company Tracker #PharmaFlow, 331 News

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DROPS

Dosage Strength

80MG/ML

Approval Date

Brand Name

INFANTS' TYLENOL

Application Number

2046059

Packaging Presentation

15ML/24ML

Regulatory Information

OTC

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Canada

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TABLET

Dosage Strength

500MG

Approval Date

Brand Name

EXTRA STRENGTH SINUTAB SINUS NIGHTTIME

Application Number

2215241

Packaging Presentation

6

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TABLET

Dosage Strength

500MG

Approval Date

Brand Name

BENYLIN EXTRA STRENGTH ALL-IN-ONE COLD, FLU & COUGH

Application Number

2218186

Packaging Presentation

24

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SUSPENSION

Dosage Strength

160MG/5ML

Approval Date

Brand Name

CHILDREN'S TYLENOL COLD

Application Number

2039982

Packaging Presentation

100ML

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TABLET

Dosage Strength

325MG

Approval Date

Brand Name

TYLENOL REGULAR STRENGTH CAPLETS

Application Number

723894

Packaging Presentation

24/50/100/200

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Dosage Strength

500MG

Approval Date

Brand Name

TYLENOL EXTRA STRENGTH CAPLETS

Application Number

723908

Packaging Presentation

10/24/50/100/150

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Dosage Strength

500MG

Approval Date

Brand Name

EXTRA STRENGTH SINUTAB SINUS & ALLERGY

Application Number

1986988

Packaging Presentation

24

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Dosage Strength

500MG

Approval Date

Brand Name

EXTRA STRENGTH SINUTAB SINUS DAYTIME

Application Number

1938371

Packaging Presentation

12/24/30

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Dosage Strength

325MG

Approval Date

Brand Name

TYLENOL REGULAR STRENGTH

Application Number

559393

Packaging Presentation

12/24/50/100/500

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TABLET

Dosage Strength

500MG

Approval Date

Brand Name

TYLENOL RAPID RELEASE

Application Number

863270

Packaging Presentation

80

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Dosage Strength

160MG/5ML

Approval Date

Brand Name

CHILDREN'S TYLENOL COLD & STUFFY NOSE

Application Number

2229538

Packaging Presentation

100ML

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Dosage Strength

500MG

Approval Date

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EXTRA STRENGTH SUDAFED HEAD COLD & SINUS

Application Number

2239159

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TABLET (EXTENDED-RELEASE)

Dosage Strength

650MG

Approval Date

Brand Name

TYLENOL ARTHRITIS PAIN 8H

Application Number

2238885

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24/50/100/170

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SYRUP

Dosage Strength

500MG/15ML

Approval Date

Brand Name

BENYLIN EXTRA STRENGTH ALL-IN-ONE COUGH, COLD & FLU NIGHT

Application Number

2252376

Packaging Presentation

170ML/270ML

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Dosage Strength

160MG/5ML

Approval Date

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CHILDREN'S TYLENOL COLD AND COUGH

Application Number

2039990

Packaging Presentation

100ML

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160MG/5ML

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CHILDREN'S TYLENOL COLD AND COUGH NIGHTTIME

Application Number

2279150

Packaging Presentation

100ML

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500MG

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EXTRA STRENGTH TYLENOL SINUS DAYTIME

Application Number

2276003

Packaging Presentation

6/12/20/40

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500MG

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EXTRA STRENGTH TYLENOL SINUS NIGHTTIME

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2276038

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4/8/20/24/30

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Dosage Strength

500MG

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EXTRA STRENGTH TYLENOL FLU NIGHTTIME

Application Number

2276046

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10

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CAPSULE

Dosage Strength

250MG

Approval Date

Brand Name

TYLENOL COMPLETE COLD, COUGH & FLU PLUS MUCUS RELIEF

Application Number

2295326

Packaging Presentation

20/40

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Dosage Strength

500MG

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EXTRA STRENGTH TYLENOL COLD DAYTIME

Application Number

2276186

Packaging Presentation

6/10/20/24/40

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Dosage Strength

500MG

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BENADRYL ALLERGY, SINUS & PAIN TOTAL

Application Number

2250993

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20

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TABLET (EXTENDED-RELEASE)

Dosage Strength

650MG

Approval Date

Brand Name

TYLENOL MUSCLE & BODY

Application Number

2246060

Packaging Presentation

72

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Dosage Strength

500MG

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TYLENOL ULTRA RELIEF

Application Number

2254468

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20/80/120

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SYRUP

Dosage Strength

500MG/15ML

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Brand Name

BENYLIN EXTRA STRENGTH ALL-IN-ONE COUGH, COLD & FLU

Application Number

2245710

Packaging Presentation

180 ML

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2256576

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24

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Dosage Strength

500MG

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Brand Name

EXTRA STRENGTH TYLENOL BACK PAIN

Application Number

2290510

Packaging Presentation

18/40

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2273462

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10

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SUSPENSION

Dosage Strength

160MG/5ML

Approval Date

Brand Name

CHILDREN'S TYLENOL COMPLETE COLD, COUGH & FEVER NIGHTTIME

Application Number

2416050

Packaging Presentation

100ML

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Dosage Strength

500MG

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EXTRA STRENGTH TYLENOL BODY PAIN NIGHT

Application Number

2357356

Packaging Presentation

2/18/40

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2276259

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4/10/16/20/40

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TABLET (CHEWABLE)

Dosage Strength

160MG

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Brand Name

CHILDREN'S TYLENOL CHEWABLES

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2241361

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20

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2478110

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18

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Application Number

2348098

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10/20/50/80

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2348071

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CAPSULE

Dosage Strength

250MG

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Brand Name

BENYLIN ALL-IN-ONE COLD, FLU & COUGH LIQUID GELS

Application Number

2345110

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20

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Dosage Strength

160MG/5ML

Approval Date

Brand Name

CHILDREN'S TYLENOL COMPLETE COLD, COUGH & FEVER

Application Number

2376474

Packaging Presentation

100ML

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Dosage Strength

325MG

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Brand Name

TYLENOL LIQUID GELS

Application Number

2407612

Packaging Presentation

2/32/72/115

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Brand Name

BENYLIN EXTRA STRENGTH MUCUS & PHLEGM PLUS COLD RELIEF

Application Number

2347652

Packaging Presentation

24

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Approval Date

Brand Name

BENYLIN EXTRA STRENGTH COLD & SINUS NIGHT

Application Number

2306409

Packaging Presentation

10

Regulatory Information

OTC

Country of Registration

Canada

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ACETAMINOPHEN

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URL Supplier Web Content

Dosage Form

SYRUP

Dosage Strength

500MG/15ML

Approval Date

Brand Name

BENYLIN EXTRA STRENGTH MUCUS & PHLEGM PLUS COLD RELIEF

Application Number

2366207

Packaging Presentation

180ML

Regulatory Information

OTC

Country of Registration

Canada

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SUSPENSION

Dosage Strength

160MG/5ML

Approval Date

Brand Name

BENYLIN FOR CHILDREN ALL-IN-ONE COLD & FEVER

Application Number

2305496

Packaging Presentation

100ML

Regulatory Information

OTC

Country of Registration

Canada

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DROPS

Dosage Strength

80MG/ML

Approval Date

Brand Name

INFANTS' TYLENOL FEVER & SORE THROAT PAIN

Application Number

2389908

Packaging Presentation

24ML

Regulatory Information

OTC

Country of Registration

Canada

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SUSPENSION

Dosage Strength

160MG/5ML

Approval Date

Brand Name

CHILDREN'S TYLENOL FEVER & SORE THROAT PAIN

Application Number

2389924

Packaging Presentation

100ML

Regulatory Information

OTC

Country of Registration

Canada

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SYRUP

Dosage Strength

500MG/15ML

Approval Date

Brand Name

BENYLIN EXTRA STRENGTH ALL-IN-ONE COUGH, COLD & FLU WITH WARMING SENSATION

Application Number

2321432

Packaging Presentation

Regulatory Information

OTC

Country of Registration

Canada

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POWDER

Dosage Strength

160MG/SACHET

Approval Date

Brand Name

CHILDREN'S TYLENOL EASY DISSOLVE

Application Number

2517280

Packaging Presentation

Regulatory Information

OTC

Country of Registration

Canada

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SYRUP

Dosage Strength

1000MG/30ML

Approval Date

Brand Name

EXTRA STRENGTH TYLENOL COMPLETE COLD, COUGH & FLU PLUS MUCUS RELIEF NIGHTTIME

Application Number

2365596

Packaging Presentation

170ML

Regulatory Information

OTC

Country of Registration

Canada

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TABLET

Dosage Strength

500MG

Approval Date

Brand Name

EXTRA STRENGTH TYLENOL COMPLETE COLD, COUGH & FLU DAYTIME

Application Number

2365731

Packaging Presentation

24

Regulatory Information

OTC

Country of Registration

Canada

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TABLET

Dosage Strength

500MG

Approval Date

Brand Name

EXTRA STRENGTH TYLENOL COMPLETE COLD, COUGH & FLU NIGHTTIME

Application Number

2365766

Packaging Presentation

12/24/40

Regulatory Information

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Country of Registration

Canada

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Dosage Strength

500MG/15ML

Approval Date

Brand Name

EXTRA STRENGTH TYLENOL COMPLETE COLD, COUGH & FLU PLUS MUCUS RELIEF

Application Number

2365774

Packaging Presentation

180ML

Regulatory Information

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Country of Registration

Canada

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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

All Manufacturers, Suppliers, Distributors and Exporters of Acetaminophen with approved Health Canada of Finished Dosage Form listed on PharmaCompass.com

Acetaminophen

Acetaminophen

Synopsis

Chemistry

APIs // Active Pharmaceutical Ingredients

118 API Suppliers

84 USDMF

20 CEP/COS

16 JDMF

7 EU WC

108 KDMF

105 NDC API

28 Listed Suppliers

DEVELOPMENTS

36 Drug(s) in Development

PRICE INFORMATION

API Reference Price

API Exports

API Imports

FDF Exports

FDF Imports

DOSSIERs // Finished Dosage Formulations

2413 Dossiers

727 FDA Orange Book

482 Europe

299 Canada

73 Australia

376 South Africa

456 Listed Dossiers

DRUG PRODUCT COMPOSITION

SUPPOSITORY;RECTAL - 120MG

SUPPOSITORY;RECTAL - 325MG

SUPPOSITORY;RECTAL - 650MG

SUPPOSITORY;RECTAL - 80MG

CAPSULE;ORAL - 325MG;50MG;40MG;30MG

TABLET, EXTENDED RELEASE;ORAL - 325MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

TABLET;ORAL - 250MG;250MG;65MG

TABLET;ORAL - 325MG;37.5MG

SOLUTION;INTRAVENOUS - 1GM/100ML (10MG/ML)

TABLET;ORAL - 300MG;15MG

TABLET;ORAL - 300MG;30MG

TABLET;ORAL - 300MG;60MG

TABLET;ORAL - 325MG;5MG

TABLET;ORAL - 325MG;50MG;40MG

TABLET;ORAL - 300MG;60MG

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TABLET, EXTENDED RELEASE;ORAL - 325MG;7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons