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clindamycin hydrochloride - 64720-153-10 - (clindamycin hydrochloride)

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Drug Information of clindamycin hydrochloride

Product NDC: 64720-153
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, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of clindamycin hydrochloride

Product NDC: 64720-153
Labeler Name: CorePharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065194
Marketing Category: ANDA
Start Marketing Date: 20040415

Package Information of clindamycin hydrochloride

Package NDC: 64720-153-10
Package Description: 100 CAPSULE, GELATIN COATED in 1 BOTTLE (64720-153-10)

NDC Information of clindamycin hydrochloride

NDC Code 64720-153-10
Proprietary Name clindamycin hydrochloride
Package Description 100 CAPSULE, GELATIN COATED in 1 BOTTLE (64720-153-10)
Product NDC 64720-153
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clindamycin hydrochloride
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20040415
Marketing Category Name ANDA
Labeler Name CorePharma, LLC
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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