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Clindamycin Hydrochloride - 63629-2817-6 - (Clindamycin Hydrochloride)

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Drug Information of Clindamycin Hydrochloride

Product NDC: 63629-2817
Proprietary Name: Clindamycin Hydrochloride
Non Proprietary Name: Clindamycin Hydrochloride
Active Ingredient(s): 150    mg/1 & nbsp;   Clindamycin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Clindamycin Hydrochloride

Product NDC: 63629-2817
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA063083
Marketing Category: ANDA
Start Marketing Date: 19910731

Package Information of Clindamycin Hydrochloride

Package NDC: 63629-2817-6
Package Description: 21 CAPSULE in 1 BOTTLE (63629-2817-6)

NDC Information of Clindamycin Hydrochloride

NDC Code 63629-2817-6
Proprietary Name Clindamycin Hydrochloride
Package Description 21 CAPSULE in 1 BOTTLE (63629-2817-6)
Product NDC 63629-2817
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clindamycin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19910731
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name CLINDAMYCIN HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient]

Complete Information of Clindamycin Hydrochloride


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