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Demeclocycline Hydrochloride - 65162-555-48 - (Demeclocycline Hydrochloride)

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Drug Information of Demeclocycline Hydrochloride

Product NDC: 65162-555
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: 65162-555
Labeler Name: Amneal Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065425
Marketing Category: ANDA
Start Marketing Date: 20100401

Package Information of Demeclocycline Hydrochloride

Package NDC: 65162-555-48
Package Description: 48 TABLET in 1 BOTTLE (65162-555-48)

NDC Information of Demeclocycline Hydrochloride

NDC Code 65162-555-48
Proprietary Name Demeclocycline Hydrochloride
Package Description 48 TABLET in 1 BOTTLE (65162-555-48)
Product NDC 65162-555
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Demeclocycline Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100401
Marketing Category Name ANDA
Labeler Name Amneal 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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