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USFDA APPLICATION NUMBER - 202880 / DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 40MG
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| Hydrocodone Bitartrate(UNII: NO70W886KK) (Hydrocodone - UNII:6YKS4Y3WQ7) | Hydrocodone Bitartrate | 50mg | 40mg | 30mg | 20mg | 15mg | 10mg |
Inactive Ingredients
| Ingredient Name | Persion Pharmaceuticals LLC |
|---|---|
| Ammonio Methacrylate Copolymer Type B(161H3B14U2) | |
| FD&C Blue No. 1(H3R47K3TBD) | |
| FD&C Red No. 3(PN2ZH5LOQY) | |
| FD&C Red No. 40(WZB9127XOA) | |
| Ferric Oxide Red(1K09F3G675) | |
| Ferric Oxide Yellow(EX438O2MRT) | |
| Ferrosoferric Oxide(XM0M87F357) | |
| Gelatin, Unspecified(2G86QN327L) | |
| HYPROMELLOSE, UNSPECIFIED(3NXW29V3WO) | |
| POLYETHYLENE GLYCOL, UNSPECIFIED(3WJQ0SDW1A) | |
| Povidone, Unspecified(FZ989GH94E) | |
| Silicon Dioxide(ETJ7Z6XBU4) | |
| Sucrose(C151H8M554) | |
| Talc(7SEV7J4R1U) | |
| Titanium Dioxide(15FIX9V2JP) |
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