Product NDC: | 24236-167 |
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) |
Product NDC: | 24236-167 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065061 |
Marketing Category: | ANDA |
Start Marketing Date: | 20101216 |
Package NDC: | 24236-167-24 |
Package Description: | 200 CAPSULE in 1 CANISTER (24236-167-24) |
NDC Code | 24236-167-24 |
Proprietary Name | CLINDAMYCIN HYDROCHLORIDE |
Package Description | 200 CAPSULE in 1 CANISTER (24236-167-24) |
Product NDC | 24236-167 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CLINDAMYCIN HYDROCHLORIDE |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20101216 |
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] |