
Reset all filters
01 1ABRAXIS PHARM
02 2Adcock Ingram
03 6American Regent
04 2Apotex Inc
05 1Appasamy Associates
06 3Aspiro Pharma
07 1Aurolab
08 1Bahrain Pharma
09 1BioPhausia AB
10 2Briyosis Soft Caps
11 4Church & Dwight Co
12 3DOMINION VETERINARY LABORATORIES LTD.
13 1Eloge
14 4Farbe Firma
15 1Farmigea
16 1Flagship Biotech International Pvt. Ltd
17 2Fresenius Kabi Austria
18 3Fresenius Kabi USA
19 5Fresenius SE & Co. KGaA
20 3GLAND PHARMA LIMITED
21 1Globofarm International
22 1Hanlim Pharmaceuticals Inc
23 1IDI FARMACEUTICI Srl
24 2Johnson & Johnson
25 2Juno Pharmaceuticals Pty Ltd
26 1Karo Pharma
27 1Mahban Group
28 3Nivagen
29 4ODAN LABORATORIES LTD
30 3Pharmascience Inc.
31 1Prestige Consumer Healthcare
32 3RK Pharma
33 1S.A. Alcon-Couvreur N.V.
34 13Sandoz B2B
35 2Smith & Kenner Pharmaceuticals
36 2Somerset Pharmaceuticals Inc
37 1Themis Medicare
38 2Vefa Ilac
39 1Vega Biotech Pvt. Ltd.
40 1Wellcopharma
41 1Yash Pharma Laboratories
42 2ZRS LABS
43 2Zim Laboratories
44 3Zydus Pharmaceuticals
Reset all filters
01 2CAPSULE
02 4Capsule
03 2DC Granules and Tablets
04 2DROPS
05 1EYE DROP
06 1Effervescent Tablet
07 2Eye Drop
08 1Eye Drops
09 5INF
10 1INJECTABLE;INJECTION
11 4Injection
12 4LIQUID
13 1NAS
14 6OINTMENT
15 1OPD
16 1Oral Solution
17 2POWDER
18 1Pellet
19 14SOLUTION
20 28SOLUTION;INTRAVENOUS
21 5SUPPOSITORY
22 1SYRUP
23 2TABLET
24 6Tablet
25 1Topical Suspension
26 1Uncoated dispersable tablet
27 2Blank
Reset all filters
01 1Approved
02 1DISCN
03 1Deregistered
04 15Ethical
05 9Generic
06 10NON-PRESCRIPTION DRUGS
07 1OTC
08 4Originator
09 8Prescription
10 28RX
11 23Blank
Reset all filters
01 18-SYMPTOM RELIEF
02 1ALLERGY EYE DROPS
03 1ANC
04 1ANODAN-HC 10MG SUPPOSITORIES
05 1ANODAN-HC OINTMENT
06 1ANUSOL PLUS OINTMENT
07 1ANUSOL PLUS SUPPOSITORIES
08 1ANUSOL-HC OINTMENT
09 1ANUSOL-HC SUPPOSITORIES
10 1CLEAR EYES ALLERGY
11 1Cozic
12 2EGOZINC-HC
13 1Eurofar
14 1Feredet XT
15 1Franbio
16 1HEMORRHOIDAL OINTMENT
17 1Hiner-Z
18 1MICRO +4 REGULAR STRENGTH
19 3MICRO PLUS 6 (PEDIATRIC)
20 1MICRO SE
21 2MICRO ZN
22 2MICRO+ TE PEDIATRIC
23 2MICRO+6 CONCENTRATE
24 2MICRO+6 REGULAR
25 1MULTRYS
26 1Mebopan
27 1Nazene Z Nasal Spray
28 1Oculosan
29 1PROCTODAN-HC OINTMENT
30 1PROCTODAN-HC SUPPOSITORIES
31 1QUENCH LYTE
32 1RELIEF A.C
33 4SMOFKABIVEN
34 1SMOFKABIVEN PERIPHERAL
35 1Solvezinc
36 1Solvezink
37 2TRALEMENT
38 1VISINE FOR ALLERGY 3 SYMPTOM RELIEF
39 1VISINE MULTI-SYMPTOM
40 1Vitawell Vit C + Zinc
41 2WHITE LOTION TAB
42 26ZINC SULFATE
43 2ZINC SULFATE INJECTION, USP
44 1Zinc Imizol
45 1Zinc Sulphate
46 1Zincfrin
47 1Zinconet C
48 1Zinfate
49 15Blank
Reset all filters
01 1Bahrain
02 34Canada
03 1Guatemala
04 19India
05 1Iran
06 2Italy
07 1Norway
08 7South Africa
09 1South Korea
10 2Sweden
11 2Turkey
12 29USA
13 1Vietnam
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG ZINC/ML
Packaging :
Approval Date : 1987-05-05
Application Number : 19229
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
CUPRIC SULFATE; MANGANESE SULFATE; SELENIOUS ACID; ZINC SULFATE
Brand Name : TRALEMENT
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 0.3MG COPPER/ML;EQ 55MCG BASE/ML;EQ 60MCG SELENIUM/ML;EQ 3MG BASE/ML (1ML)
Packaging :
Approval Date : 2020-07-02
Application Number : 209376
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
CUPRIC SULFATE; MANGANESE SULFATE; SELENIOUS ACID; ZINC SULFATE
Brand Name : TRALEMENT
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 0.3MG COPPER/ML;EQ 55MCG BASE/ML;EQ 60MCG SELENIUM/ML;EQ 3MG BASE/ML (5ML)
Packaging :
Approval Date : 2020-12-02
Application Number : 209376
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
CUPRIC SULFATE; MANGANESE SULFATE; SELENIOUS ACID; ZINC SULFATE
Brand Name : MULTRYS
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 60MCG COPPER/ML;EQ 3MCG BASE/ML;EQ 6MCG SELENIUM/ML;EQ 1000MCG BASE/ML (1ML)
Packaging :
Approval Date : 2021-06-30
Application Number : 209376
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 30MG BASE/10ML (EQ 3MG BASE/ML)
Packaging :
Approval Date : 2019-07-18
Application Number : 209377
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 25MG BASE/5ML (EQ 5MG BASE/ML)
Packaging :
Approval Date : 2019-07-18
Application Number : 209377
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 10MG BASE/10ML (EQ 1MG BASE/ML)
Packaging :
Approval Date : 2020-04-15
Application Number : 209377
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 10MG BASE/10ML (EQ 1MG BASE/ML)
Packaging :
Approval Date : 2022-12-27
Application Number : 216145
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 25MG BASE/5ML (EQ 5MG BASE/ML)
Packaging :
Approval Date : 2022-12-27
Application Number : 216145
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 30MG BASE/10ML (EQ 3MG BASE/ML)
Packaging :
Approval Date : 2022-12-27
Application Number : 216145
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 25MG BASE/5ML (EQ 5MG BASE/ML)
Packaging :
Approval Date : 2022-05-03
Application Number : 216249
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 30MG BASE/10ML (EQ 3MG BASE/ML)
Packaging :
Approval Date : 2022-05-03
Application Number : 216249
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 10MG BASE/10ML (EQ 1MG BASE/ML)
Packaging :
Approval Date : 2023-09-01
Application Number : 216249
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 10MG BASE/10ML (EQ 1MG BASE/ML)
Packaging :
Approval Date : 2024-07-05
Application Number : 214597
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 25MG BASE/5ML (EQ 5MG BASE/ML)
Packaging :
Approval Date : 2024-07-05
Application Number : 214597
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 30MG BASE/10ML (EQ 3MG BASE/ML)
Packaging :
Approval Date : 2024-07-05
Application Number : 214597
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 25MG BASE/5ML (EQ 5MG BASE/ML)
Packaging :
Approval Date : 2024-07-17
Application Number : 216135
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 30MG BASE/10ML (EQ 3MG BASE/ML)
Packaging :
Approval Date : 2024-07-17
Application Number : 216135
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 10MG BASE/10ML (EQ 1MG BASE/ML)
Packaging :
Approval Date : 2023-08-22
Application Number : 217074
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ZINC SULFATE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : EQ 25MG BASE/5ML (EQ 5MG BASE/ML)
Packaging :
Approval Date : 2023-08-22
Application Number : 217074
Regulatory Info : RX
Registration Country : USA