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clindamycin hydrochloride
clindamycin hydrochloride - 59762-5010-2 - (CLINDAMYCIN HYDROCHLORIDE)
Drug Information of clindamycin hydrochloride
| Product NDC: | 59762-5010 |
| 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: | 59762-5010 |
| 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: | 59762-5010-2 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (59762-5010-2) |
NDC Information of clindamycin hydrochloride
| NDC Code | 59762-5010-2 |
| Proprietary Name | clindamycin hydrochloride |
| Package Description | 100 CAPSULE in 1 BOTTLE (59762-5010-2) |
| Product NDC | 59762-5010 |
| 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 | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient] |
