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Clindamycin hydrochloride
Clindamycin hydrochloride - 68788-9942-2 - (Clindamycin hydrochloride)
Drug Information of Clindamycin hydrochloride
| Product NDC: | 68788-9942 |
| 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: | 68788-9942 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065061 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120116 |
Package Information of Clindamycin hydrochloride
| Package NDC: | 68788-9942-2 |
| Package Description: | 20 CAPSULE in 1 BOTTLE (68788-9942-2) |
NDC Information of Clindamycin hydrochloride
| NDC Code | 68788-9942-2 |
| Proprietary Name | Clindamycin hydrochloride |
| Package Description | 20 CAPSULE in 1 BOTTLE (68788-9942-2) |
| Product NDC | 68788-9942 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Clindamycin hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120116 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred 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] |
