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Clindamycin Hydrochloride - 0527-1381-04 - (Clindamycin Hydrochloride)

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Drug Information of Clindamycin Hydrochloride

Product NDC: 0527-1381
Proprietary Name: Clindamycin Hydrochloride
Non Proprietary Name: Clindamycin Hydrochloride
Active Ingredient(s): 75    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: 0527-1381
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065242
Marketing Category: ANDA
Start Marketing Date: 20050812

Package Information of Clindamycin Hydrochloride

Package NDC: 0527-1381-04
Package Description: 200 CAPSULE in 1 BOTTLE (0527-1381-04)

NDC Information of Clindamycin Hydrochloride

NDC Code 0527-1381-04
Proprietary Name Clindamycin Hydrochloride
Package Description 200 CAPSULE in 1 BOTTLE (0527-1381-04)
Product NDC 0527-1381
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clindamycin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050812
Marketing Category Name ANDA
Labeler Name Lannett Company, Inc.
Substance Name CLINDAMYCIN HYDROCHLORIDE
Strength Number 75
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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