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Minocycline Hydrochloride - 55289-202-30 - (Minocycline Hydrochloride)

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Drug Information of Minocycline Hydrochloride

Product NDC: 55289-202
Proprietary Name: Minocycline Hydrochloride
Non Proprietary Name: Minocycline Hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   Minocycline Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Minocycline Hydrochloride

Product NDC: 55289-202
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA063181
Marketing Category: ANDA
Start Marketing Date: 19911230

Package Information of Minocycline Hydrochloride

Package NDC: 55289-202-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (55289-202-30)

NDC Information of Minocycline Hydrochloride

NDC Code 55289-202-30
Proprietary Name Minocycline Hydrochloride
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (55289-202-30)
Product NDC 55289-202
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Minocycline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19911230
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name MINOCYCLINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Minocycline Hydrochloride


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