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Clindamycin Hydrochloride - 67046-085-21 - (Clindamycin Hydrochloride)

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Drug Information of Clindamycin Hydrochloride

Product NDC: 67046-085
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: 67046-085
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065194
Marketing Category: ANDA
Start Marketing Date: 20100702

Package Information of Clindamycin Hydrochloride

Package NDC: 67046-085-21
Package Description: 21 CAPSULE, GELATIN COATED in 1 BLISTER PACK (67046-085-21)

NDC Information of Clindamycin Hydrochloride

NDC Code 67046-085-21
Proprietary Name Clindamycin Hydrochloride
Package Description 21 CAPSULE, GELATIN COATED in 1 BLISTER PACK (67046-085-21)
Product NDC 67046-085
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clindamycin Hydrochloride
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20100702
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
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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