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Clindamycin hydrochloride - 54868-5211-2 - (Clindamycin hydrochloride)

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Drug Information of Clindamycin hydrochloride

Product NDC: 54868-5211
Proprietary Name: Clindamycin hydrochloride
Non Proprietary Name: Clindamycin hydrochloride
Active Ingredient(s): 300    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: 54868-5211
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065061
Marketing Category: ANDA
Start Marketing Date: 20050419

Package Information of Clindamycin hydrochloride

Package NDC: 54868-5211-2
Package Description: 40 CAPSULE in 1 BOTTLE, PLASTIC (54868-5211-2)

NDC Information of Clindamycin hydrochloride

NDC Code 54868-5211-2
Proprietary Name Clindamycin hydrochloride
Package Description 40 CAPSULE in 1 BOTTLE, PLASTIC (54868-5211-2)
Product NDC 54868-5211
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clindamycin hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050419
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CLINDAMYCIN HYDROCHLORIDE
Strength Number 300
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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