USFDA APPLICATION NUMBER - 50795 / DOSAGE - TABLET, DELAYED RELEASE;ORAL - EQ 80MG BASE
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
DOXYCYCLINE HYCLATE(UNII: 19XTS3T51U) (DOXYCYCLINE ANHYDROUS - UNII:334895S862) | DOXYCYCLINE ANHYDROUS | 75mg in 100 |
Inactive Ingredients
Ingredient Name | Allergan, Inc. | Mayne Pharma International Pty Ltd | Mylan Pharmaceuticals Inc. |
---|---|---|---|
ANHYDROUS LACTOSE(3SY5LH9PMK) | |||
CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | |||
CROSPOVIDONE (15 MPA.S AT 5%)(68401960MK) | |||
CROSPOVIDONE(2S7830E561) | |||
CROSPOVIDONE(68401960MK) | |||
CROSPOVIDONE, UNSPECIFIED(2S7830E561) | |||
HYPROMELLOSE PHTHALATE (24% PHTHALATE, 55 CST)(87Y6436BKR) | |||
LACTOSE MONOHYDRATE(EWQ57Q8I5X) | |||
MAGNESIUM STEARATE(70097M6I30) | |||
POVIDONE, UNSPECIFIED(FZ989GH94E) | |||
POVIDONES(FZ989GH94E) | |||
SILICON DIOXIDE(ETJ7Z6XBU4) | |||
SODIUM CHLORIDE(451W47IQ8X) | |||
SODIUM LAURYL SULFATE(368GB5141J) | |||
STARCH, CORN(O8232NY3SJ) | |||
STEARIC ACID(4ELV7Z65AP) | |||
TALC(7SEV7J4R1U) | |||
TRIETHYL CITRATE(8Z96QXD6UM) |
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