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clindamycin hydrochloride - 68084-244-01 - (clindamycin hydrochloride)

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Drug Information of clindamycin hydrochloride

Product NDC: 68084-244
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: 68084-244
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065061
Marketing Category: ANDA
Start Marketing Date: 20080422

Package Information of clindamycin hydrochloride

Package NDC: 68084-244-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-244-01) > 10 CAPSULE in 1 BLISTER PACK (68084-244-11)

NDC Information of clindamycin hydrochloride

NDC Code 68084-244-01
Proprietary Name clindamycin hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (68084-244-01) > 10 CAPSULE in 1 BLISTER PACK (68084-244-11)
Product NDC 68084-244
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clindamycin hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20080422
Marketing Category Name ANDA
Labeler Name American Health Packaging
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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