| NDC Code | 21695-723-14 |
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| Package Description | 14 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (21695-723-14) |
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| Product NDC | 21695-723 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Amrix |
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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 | 20071001 |
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| Marketing Category Name | NDA |
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| Application Number | NDA021777 |
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| Manufacturer | Rebel Distributors Corp. |
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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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