| NDC Code | 69306-015-03 |
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| Package Description | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69306-015-03) |
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| Product NDC | 69306-015 |
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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, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20190304 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA021777 |
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| Manufacturer | Doc Rx |
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| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
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| Strength | 15 |
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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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