Home > National Drug Code (NDC) > Primaquine Phosphate

Primaquine Phosphate - 43063-225-28 - (Primaquine Phosphate)

Alphabetical Index


Drug Information of Primaquine Phosphate

Product NDC: 43063-225
Proprietary Name: Primaquine Phosphate
Non Proprietary Name: Primaquine Phosphate
Active Ingredient(s): 26.3    mg/1 & nbsp;   Primaquine Phosphate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Primaquine Phosphate

Product NDC: 43063-225
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA008316
Marketing Category: ANDA
Start Marketing Date: 20100101

Package Information of Primaquine Phosphate

Package NDC: 43063-225-28
Package Description: 28 TABLET in 1 BOTTLE, PLASTIC (43063-225-28)

NDC Information of Primaquine Phosphate

NDC Code 43063-225-28
Proprietary Name Primaquine Phosphate
Package Description 28 TABLET in 1 BOTTLE, PLASTIC (43063-225-28)
Product NDC 43063-225
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Primaquine Phosphate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100101
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name PRIMAQUINE PHOSPHATE
Strength Number 26.3
Strength Unit mg/1
Pharmaceutical Classes Antimalarial [EPC]

Complete Information of Primaquine Phosphate


General Information