Isoniazid - 55289-742-01 - (Isoniazid)

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Drug Information of Isoniazid

Product NDC: 55289-742
Proprietary Name: Isoniazid
Non Proprietary Name: Isoniazid
Active Ingredient(s): 300    mg/1 & nbsp;   Isoniazid
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Isoniazid

Product NDC: 55289-742
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087425
Marketing Category: ANDA
Start Marketing Date: 19810714

Package Information of Isoniazid

Package NDC: 55289-742-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (55289-742-01)

NDC Information of Isoniazid

NDC Code 55289-742-01
Proprietary Name Isoniazid
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (55289-742-01)
Product NDC 55289-742
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isoniazid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19810714
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name ISONIAZID
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Antimycobacterial [EPC]

Complete Information of Isoniazid


General Information