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Demeclocycline Hydrochloride - 0904-6181-96 - (Demeclocycline Hydrochloride)

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Drug Information of Demeclocycline Hydrochloride

Product NDC: 0904-6181
Proprietary Name: Demeclocycline Hydrochloride
Non Proprietary Name: Demeclocycline Hydrochloride
Active Ingredient(s): 300    mg/1 & nbsp;   Demeclocycline Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Demeclocycline Hydrochloride

Product NDC: 0904-6181
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065425
Marketing Category: ANDA
Start Marketing Date: 20101119

Package Information of Demeclocycline Hydrochloride

Package NDC: 0904-6181-96
Package Description: 48 TABLET in 1 BOTTLE (0904-6181-96)

NDC Information of Demeclocycline Hydrochloride

NDC Code 0904-6181-96
Proprietary Name Demeclocycline Hydrochloride
Package Description 48 TABLET in 1 BOTTLE (0904-6181-96)
Product NDC 0904-6181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Demeclocycline Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101119
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name DEMECLOCYCLINE HYDROCHLORIDE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Antimicrobial [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Demeclocycline Hydrochloride


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