Reset all filters
01 1ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
02 5ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
03 1ACRIVASTINE; PSEUDOEPHEDRINE HYDROCHLORIDE
04 7ALPROSTADIL
05 1ASPIRIN; OXYCODONE HYDROCHLORIDE
06 2ASPIRIN; OXYCODONE HYDROCHLORIDE; OXYCODONE TEREPHTHALATE
07 1Acetylsalicylic Acid; Dipyridamole
08 2BETHANECHOL CHLORIDE
09 10CENOBAMATE
10 1CLINDAMYCIN PHOSPHATE
11 2CLIOQUINOL
12 2CYANOCOBALAMIN
13 1CYPROTERONE ACETATE
14 1DALBAVANCIN (DALBAVANCIN HYDROCHLORIDE)
15 2DANTROLENE SODIUM
16 3DEXTROAMPHETAMINE SULFATE
17 2DOXEPIN (DOXEPIN HYDROCHLORIDE)
18 1ETHINYL ESTRADIOL
19 1FLUDROCORTISONE 21-ACETATE
20 2FLUMETHASONE PIVALATE
21 1FOMEPIZOLE
22 1FOSFOMYCIN (FOSFOMYCIN TROMETHAMINE)
23 2FROVATRIPTAN (FROVATRIPTAN SUCCINATE)
24 1FROVATRIPTAN SUCCINATE
25 2HISTRELIN ACETATE
26 1ISOSORBIDE DINITRATE
27 2LABETALOL HYDROCHLORIDE
28 1MEGESTROL ACETATE
29 8METHADONE HYDROCHLORIDE
30 1METHIMAZOLE
31 2METHOCARBAMOL
32 2METHOXYFLURANE
33 2MORPHINE SULFATE
34 3NITROGLYCERIN
35 7OXYMORPHONE HYDROCHLORIDE
36 2PENBUTOLOL SULFATE
37 2PITOLISANT HYDROCHLORIDE
38 1PIZOTIFEN (PIZOTIFEN MALATE)
39 1PROPYLTHIOURACIL
40 1SINECATECHINS
41 2SUMATRIPTAN SUCCINATE
42 3TACROLIMUS
43 8TAPENTADOL (TAPENTADOL HYDROCHLORIDE)
44 4TESTOSTERONE
45 1TESTOSTERONE UNDECANOATE
46 4THEOPHYLLINE
47 3TRAMADOL HYDROCHLORIDE
48 1Testosteron
49 1Testosterone
50 1VALRUBICIN
51 3Zonisamide
Reset all filters
01 2BOCA PHARMA LLC
02 46ENDO OPERATIONS
03 68ENDO OPERATIONS LTD.
04 5Endo Ventures Limited
05 1Endo Ventures Unlimited Company
Reset all filters
01 1CAPSULE
02 2CAPSULE (SUSTAINED-RELEASE)
03 5CAPSULE, EXTENDED RELEASE;ORAL
04 1CAPSULE;ORAL
05 2CREAM
06 1Capsule For Inhalation
07 2DROPS
08 1GEL
09 1GEL, METERED;NASAL
10 1GEL, METERED;TRANSDERMAL
11 1GEL;TRANSDERMAL
12 3Hard Capsule
13 2IMPLANT;SUBCUTANEOUS
14 7INJECTABLE;INJECTION
15 1INJECTABLE;INTRAMUSCULAR
16 2INJECTABLE;SUBCUTANEOUS
17 5KIT
18 1LIQUID
19 1OINTMENT
20 3PATCH
21 1PELLET;IMPLANTATION
22 3POWDER FOR SOLUTION
23 5SOLUTION
24 1SOLUTION;INTRAVESICAL
25 1SOLUTION;TOPICAL
26 1SPRAY, METERED;NASAL
27 1SUSPENSION;ORAL
28 28TABLET
29 11TABLET (EXTENDED-RELEASE)
30 3TABLET (IMMEDIATE RELEASE)
31 7TABLET, EXTENDED RELEASE;ORAL
32 15TABLET;ORAL
33 2Transdermal Gel
Reset all filters
01 10.005MG/VIAL
02 20.01MG/VIAL
03 10.02%/W/V
04 10.02%/W/W
05 20.02MG/VIAL
06 10.035MG
07 20.04MG/VIAL
08 10.1MG
09 10.2MG/HOUR
10 10.4MG/HOUR
11 10.5MG/INH
12 10.5MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
13 10.6MG/HOUR
14 10.75MG
15 11%
16 11%/W/V
17 110%/W/W
18 8100MG
19 510MG
20 210MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 110MG/0.5GM ACTUATION **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 210MG/ML
23 212.5MG
24 1125MG/ML
25 2150MG
26 115MG
27 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
28 11G/ML
29 31MG
30 21MG/ML
31 22.5MG
32 5200MG
33 1200mg;25mg
34 120MG
35 220MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
36 120MG/VIAL
37 1250MG
38 625MG
39 12MG
40 13%/W/W
41 2300MG
42 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
43 1325MG;10MG
44 1325MG;2.25MG;0.19MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
45 1325MG;2.5MG
46 1325MG;4.5MG;0.38MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
47 1325MG;4.8355MG
48 1325MG;5MG
49 1325MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
50 1325MG;7.5MG
51 13G/SACHET
52 13MG
53 1400MG
54 140MG
55 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
56 140MG/ML
57 14MG
58 1500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
59 1500MG/VIAL
60 950MG
61 150MG/5GM PACKET
62 150mg
63 45MG
64 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
65 16MG
66 17.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
67 1712.8MG;60MG;32MG
68 1750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
69 1750MG/3ML (250MG/ML)
70 275MG
71 18MG;60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
72 299.9%
73 1EQ 1% BASE
74 1EQ 2.5MG BASE
75 1EQ 4MG BASE/0.5ML (EQ 8MG BASE/ML)
76 1EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
Reset all filters
01 68Canada
02 3Malta
03 1Spain
04 2Sweden
05 48USA
Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : ACETAMINOPHEN, CAFFEINE, ...
Dosage Strength : 712.8MG;60MG;32MG
Packaging :
Approval Date : 2007-04-03
Application Number : 40701
Regulatory Info : DISCN
Registration Country : USA

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : RX
Registration Country : USA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : PERCOCET
Dosage Strength : 325MG;2.5MG
Packaging :
Approval Date : 1999-06-25
Application Number : 40330
Regulatory Info : RX
Registration Country : USA

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : RX
Registration Country : USA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : PERCOCET
Dosage Strength : 325MG;5MG
Packaging :
Approval Date : 1999-06-25
Application Number : 40330
Regulatory Info : RX
Registration Country : USA

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : RX
Registration Country : USA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : PERCOCET
Dosage Strength : 325MG;7.5MG
Packaging :
Approval Date : 2001-11-23
Application Number : 40330
Regulatory Info : RX
Registration Country : USA

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : RX
Registration Country : USA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : PERCOCET
Dosage Strength : 325MG;10MG
Packaging :
Approval Date : 2001-11-23
Application Number : 40330
Regulatory Info : RX
Registration Country : USA

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : PERCOCET
Dosage Strength : 325MG;5MG **Federal Re...
Packaging :
Approval Date : 1982-01-01
Application Number : 85106
Regulatory Info : DISCN
Registration Country : USA

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : Deregistered
Registration Country : Sweden
Acetylsalicylic Acid; Dipyridamole
Dosage Form : Capsule For Inhalation
Brand Name : Atranipar
Dosage Strength : 200mg;25mg
Packaging :
Approval Date : 2017-09-22
Application Number : 20150417000019
Regulatory Info : Deregistered
Registration Country : Sweden

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : DISCN
Registration Country : USA
ACRIVASTINE; PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Brand Name : SEMPREX-D
Dosage Strength : 8MG;60MG **Federal Reg...
Packaging :
Approval Date : 1994-03-25
Application Number : 19806
Regulatory Info : DISCN
Registration Country : USA

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : EDEX
Dosage Strength : 0.005MG/VIAL
Packaging :
Approval Date : 1997-06-12
Application Number : 20649
Regulatory Info : DISCN
Registration Country : USA

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : EDEX
Dosage Strength : 0.01MG/VIAL
Packaging :
Approval Date : 1997-06-12
Application Number : 20649
Regulatory Info : RX
Registration Country : USA

Endo International is a supplier offers 1 products (APIs, Excipients or Intermediates).
Find a price of Glycopyrronium Bromide bulk offered by Endo International