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USFDA APPLICATION NUMBER - 50754 / DOSAGE - TABLET;ORAL - 875MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| AMOXICILLIN(UNII: 804826J2HU) (AMOXICILLIN ANHYDROUS - UNII:9EM05410Q9) | AMOXICILLIN ANHYDROUS | 875mg |
Inactive Ingredients
| Ingredient Name | Direct Rx | Dr Reddys Laboratories Inc | Proficient Rx LP |
|---|---|---|---|
| CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | |||
| CROSPOVIDONE (15 MPA.S AT 5%)(68401960MK) | |||
| CROSPOVIDONE(2S7830E561) | |||
| CROSPOVIDONE(68401960MK) | |||
| D&C RED NO. 30(2S42T2808B) | |||
| FD&C RED NO. 3(PN2ZH5LOQY) | |||
| HYPROMELLOSE 2910 (5 MPA.S)(R75537T0T4) | |||
| MAGNESIUM STEARATE(70097M6I30) | |||
| MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |||
| POLYETHYLENE GLYCOL, UNSPECIFIED(3WJQ0SDW1A) | |||
| POLYETHYLENE GLYCOLS(3WJQ0SDW1A) | |||
| SILICON DIOXIDE(ETJ7Z6XBU4) | |||
| SODIUM BENZOATE(OJ245FE5EU) | |||
| SODIUM CITRATE(1Q73Q2JULR) | |||
| SODIUM CITRATE, UNSPECIFIED FORM(1Q73Q2JULR) | |||
| SODIUM STARCH GLYCOLATE TYPE A POTATO(5856J3G2A2) | |||
| SODIUM(9NEZ333N27) | |||
| SUCROSE(C151H8M554) | |||
| TITANIUM DIOXIDE(15FIX9V2JP) | |||
| XANTHAN GUM(TTV12P4NEE) |
