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Clindamycin Hydrochloride - 49999-011-28 - (Clindamycin Hydrochloride)

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Drug Information of Clindamycin Hydrochloride

Product NDC: 49999-011
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: 49999-011
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA063083
Marketing Category: ANDA
Start Marketing Date: 20101108

Package Information of Clindamycin Hydrochloride

Package NDC: 49999-011-28
Package Description: 10 CAPSULE in 1 BOTTLE, PLASTIC (49999-011-28)

NDC Information of Clindamycin Hydrochloride

NDC Code 49999-011-28
Proprietary Name Clindamycin Hydrochloride
Package Description 10 CAPSULE in 1 BOTTLE, PLASTIC (49999-011-28)
Product NDC 49999-011
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clindamycin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101108
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products 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


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