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clindamycin palmitate hydrochloride
clindamycin palmitate hydrochloride - 59762-0016-1 - (clindamycin palmitate hydrochloride)
Drug Information of clindamycin palmitate hydrochloride
| Product NDC: | 59762-0016 |
| Proprietary Name: | clindamycin palmitate hydrochloride |
| Non Proprietary Name: | clindamycin palmitate hydrochloride |
| Active Ingredient(s): | 75 mg/5mL & nbsp; clindamycin palmitate hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of clindamycin palmitate hydrochloride
| Product NDC: | 59762-0016 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062644 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19710916 |
Package Information of clindamycin palmitate hydrochloride
| Package NDC: | 59762-0016-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (59762-0016-1) > 100 mL in 1 BOTTLE |
NDC Information of clindamycin palmitate hydrochloride
| NDC Code | 59762-0016-1 |
| Proprietary Name | clindamycin palmitate hydrochloride |
| Package Description | 1 BOTTLE in 1 CARTON (59762-0016-1) > 100 mL in 1 BOTTLE |
| Product NDC | 59762-0016 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clindamycin palmitate hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19710916 |
| Marketing Category Name | ANDA |
| Labeler Name | Greenstone LLC |
| Substance Name | CLINDAMYCIN PALMITATE HYDROCHLORIDE |
| Strength Number | 75 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient] |
