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Clindamycin Hydrochloride - 52125-434-02 - (Clindamycin Hydrochloride)

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Drug Information of Clindamycin Hydrochloride

Product NDC: 52125-434
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: 52125-434
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA063029
Marketing Category: ANDA
Start Marketing Date: 20130515

Package Information of Clindamycin Hydrochloride

Package NDC: 52125-434-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (52125-434-02)

NDC Information of Clindamycin Hydrochloride

NDC Code 52125-434-02
Proprietary Name Clindamycin Hydrochloride
Package Description 30 CAPSULE in 1 BLISTER PACK (52125-434-02)
Product NDC 52125-434
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clindamycin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130515
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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