Arestin - 65976-100-01 - (Minocycline Hydrochloride)

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Drug Information of Arestin

Product NDC: 65976-100
Proprietary Name: Arestin
Non Proprietary Name: Minocycline Hydrochloride
Active Ingredient(s): 1    mg/1 & nbsp;   Minocycline Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): POWDER
Coding System: National Drug Codes(NDC)

Labeler Information of Arestin

Product NDC: 65976-100
Labeler Name: OraPharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050781
Marketing Category: NDA
Start Marketing Date: 20110321

Package Information of Arestin

Package NDC: 65976-100-01
Package Description: 1 POWDER in 1 POUCH (65976-100-01)

NDC Information of Arestin

NDC Code 65976-100-01
Proprietary Name Arestin
Package Description 1 POWDER in 1 POUCH (65976-100-01)
Product NDC 65976-100
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Minocycline Hydrochloride
Dosage Form Name POWDER
Route Name ORAL
Start Marketing Date 20110321
Marketing Category Name NDA
Labeler Name OraPharma, Inc.
Substance Name MINOCYCLINE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Arestin


General Information