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demeclocycline hydrochloride - 61748-115-01 - (demeclocycline hydrochloride)

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Drug Information of demeclocycline hydrochloride

Product NDC: 61748-115
Proprietary Name: demeclocycline hydrochloride
Non Proprietary Name: demeclocycline hydrochloride
Active Ingredient(s): 150    mg/1 & nbsp;   demeclocycline hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of demeclocycline hydrochloride

Product NDC: 61748-115
Labeler Name: VersaPharm Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065389
Marketing Category: ANDA
Start Marketing Date: 20081215

Package Information of demeclocycline hydrochloride

Package NDC: 61748-115-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (61748-115-01)

NDC Information of demeclocycline hydrochloride

NDC Code 61748-115-01
Proprietary Name demeclocycline hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (61748-115-01)
Product NDC 61748-115
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name demeclocycline hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081215
Marketing Category Name ANDA
Labeler Name VersaPharm Incorporated
Substance Name DEMECLOCYCLINE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Antimicrobial [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of demeclocycline hydrochloride


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