USFDA APPLICATION NUMBER - 50795 / DOSAGE - TABLET, DELAYED RELEASE;ORAL - EQ 150MG 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. | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals 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) | ||||
HYPROMELLOSE 2910 (5 MPA.S)(R75537T0T4) | ||||
HYPROMELLOSE 2910 (6 MPA.S)(0WZ8WG20P6) | ||||
HYPROMELLOSE PHTHALATE (24% PHTHALATE, 55 CST)(87Y6436BKR) | ||||
HYPROMELLOSE PHTHALATE (31% PHTHALATE, 40 CST)(G4U024CQK6) | ||||
LACTOSE MONOHYDRATE(EWQ57Q8I5X) | ||||
MAGNESIUM STEARATE(70097M6I30) | ||||
POVIDONE, UNSPECIFIED(FZ989GH94E) | ||||
SILICON DIOXIDE(ETJ7Z6XBU4) | ||||
SODIUM CHLORIDE(451W47IQ8X) | ||||
SODIUM LAURYL SULFATE(368GB5141J) | ||||
STARCH, CORN(O8232NY3SJ) | ||||
STEARIC ACID(4ELV7Z65AP) | ||||
TALC(7SEV7J4R1U) | ||||
TRIACETIN(XHX3C3X673) | ||||
TRIETHYL CITRATE(8Z96QXD6UM) |
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