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Clindamycin Hydrochloride - 55289-890-56 - (Clindamycin Hydrochloride)

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Drug Information of Clindamycin Hydrochloride

Product NDC: 55289-890
Proprietary Name: Clindamycin Hydrochloride
Non Proprietary Name: Clindamycin Hydrochloride
Active Ingredient(s): 300    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: 55289-890
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA063083
Marketing Category: ANDA
Start Marketing Date: 20030318

Package Information of Clindamycin Hydrochloride

Package NDC: 55289-890-56
Package Description: 56 CAPSULE in 1 BOTTLE, PLASTIC (55289-890-56)

NDC Information of Clindamycin Hydrochloride

NDC Code 55289-890-56
Proprietary Name Clindamycin Hydrochloride
Package Description 56 CAPSULE in 1 BOTTLE, PLASTIC (55289-890-56)
Product NDC 55289-890
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clindamycin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20030318
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name CLINDAMYCIN HYDROCHLORIDE
Strength Number 300
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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