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clindamycin hydrochloride - 59762-3328-1 - (CLINDAMYCIN HYDROCHLORIDE)

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Drug Information of clindamycin hydrochloride

Product NDC: 59762-3328
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: 59762-3328
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050162
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19700522

Package Information of clindamycin hydrochloride

Package NDC: 59762-3328-1
Package Description: 100 CAPSULE in 1 BOTTLE (59762-3328-1)

NDC Information of clindamycin hydrochloride

NDC Code 59762-3328-1
Proprietary Name clindamycin hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (59762-3328-1)
Product NDC 59762-3328
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CLINDAMYCIN HYDROCHLORIDE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19700522
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone 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


General Information