Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
01 1Pharm-RX Chemical
02 1ANTARIA LTD
03 1Anmol Chemicals
04 1Brenntag
05 1Eagle Chemical
06 2Everzinc
07 1Grillo
08 1HAKUSUI TECH
09 1Jost Chemical
10 1Nitika Pharmaceutical Specialities
11 1Quality Chemicals
12 1SUL OXIDOS INDUSTRIA E COMERCIO LTDA
13 1Sakai Chemical Industries
14 1Sudeep Pharma
15 1Valaji PharmaChem
16 1Vasa Pharmachem
01 1Australia
02 2Belgium
03 1Brazil
04 1Germany
05 6India
06 2Japan
07 1Spain
08 1Switzerland
09 2U.S.A
01 3Active
02 1Inactive
03 13Blank
01 3Valid
02 14Blank
01 1217MF10467
02 1218MF11030
03 15Blank
01 1WC-0518
02 16Blank
Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32240
Submission : 2018-08-30
Status : Active
Type : II
NDC Package Code : 55570-520
Start Marketing Date : 2013-12-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26398
Submission : 2012-09-07
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34040
Submission : 2019-09-16
Status : Active
Type : II
Certificate Number : CEP 2018-254 - Rev 01
Issue Date : 2024-08-22
Type : Chemical
Substance Number : 252
Status : Valid
NDC Package Code : 72955-100
Start Marketing Date : 2019-03-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23634
Submission : 2010-05-06
Status : Inactive
Type : II
NDC Package Code : 60396-1005
Start Marketing Date : 2014-05-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R1-CEP 2017-015 - Rev 00
Issue Date : 2023-07-31
Type : Chemical
Substance Number : 252
Status : Valid
NDC Package Code : 80723-100
Start Marketing Date : 2020-10-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
Certificate Number : R1-CEP 2012-347 - Rev 01
Issue Date : 2022-04-13
Type : Chemical
Substance Number : 252
Status : Valid
NDC Package Code : 80723-100
Start Marketing Date : 2020-10-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
A Zinc Oxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zinc Oxide, including repackagers and relabelers. The FDA regulates Zinc Oxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zinc Oxide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Zinc Oxide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zinc Oxide supplier is an individual or a company that provides Zinc Oxide active pharmaceutical ingredient (API) or Zinc Oxide finished formulations upon request. The Zinc Oxide suppliers may include Zinc Oxide API manufacturers, exporters, distributors and traders.
click here to find a list of Zinc Oxide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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