| NDC Code | 70934-216-21 |
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| Package Description | 21 CAPSULE in 1 BOTTLE, PLASTIC (70934-216-21) |
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| Product NDC | 70934-216 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Clindamycin Hydrochloride |
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| Non-Proprietary Name | Clindamycin Hydrochloride |
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| Dosage Form | CAPSULE |
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| Usage | ORAL |
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| Start Marketing Date | 20181220 |
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| End Marketing Date | 20240731 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065061 |
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| Manufacturer | Denton Pharma, Inc. dba Northwind Pharmaceuticals |
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| Substance Name | CLINDAMYCIN HYDROCHLORIDE |
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| Strength | 150 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Decreased Sebaceous Gland Activity [PE], Lincosamide Antibacterial [EPC], Lincosamides [CS], Neuromuscular Blockade [PE] |
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