| NDC Code | 69336-104-11 |
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| Package Description | 1000 CAPSULE, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69336-104-11) |
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| Product NDC | 69336-104 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Cyclobenzaprine Hydrochloride |
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| Non-Proprietary Name | Cyclobenzaprine Hydrochloride |
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| Dosage Form | CAPSULE, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20161103 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078218 |
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| Manufacturer | Sterling Knight Pharmaceuticals,LLC |
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| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
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| Strength | 5 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
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