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Clindamycin Hydrochloride - 43063-394-20 - (Clindamycin Hydrochloride)

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Drug Information of Clindamycin Hydrochloride

Product NDC: 43063-394
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: 43063-394
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065242
Marketing Category: ANDA
Start Marketing Date: 20050812

Package Information of Clindamycin Hydrochloride

Package NDC: 43063-394-20
Package Description: 20 CAPSULE in 1 BOTTLE, PLASTIC (43063-394-20)

NDC Information of Clindamycin Hydrochloride

NDC Code 43063-394-20
Proprietary Name Clindamycin Hydrochloride
Package Description 20 CAPSULE in 1 BOTTLE, PLASTIC (43063-394-20)
Product NDC 43063-394
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 PD-Rx Pharmaceuticals, Inc.
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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