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FDA Drug information

Doxycycline Hyclate

Read time: 1 mins
Marketing start date: 22 Jul 2024

Summary of product characteristics


Effective Time

20221013

Version

2

Spl Product Data Elements

Doxycycline Hyclate Doxycycline Hyclate DOXYCYCLINE HYCLATE DOXYCYCLINE ANHYDROUS ANHYDROUS LACTOSE CELLULOSE, MICROCRYSTALLINE CROSPOVIDONE HYPROMELLOSE PHTHALATE (24% PHTHALATE, 55 CST) HYPROMELLOSES LACTOSE MONOHYDRATE SODIUM CHLORIDE SODIUM LAURYL SULFATE STARCH, CORN STEARIC ACID TALC TRIETHYL CITRATE WHITE TO OFF-WHITE OVAL 70;8 Doxycycline Hyclate Doxycycline Hyclate DOXYCYCLINE HYCLATE DOXYCYCLINE ANHYDROUS ANHYDROUS LACTOSE CELLULOSE, MICROCRYSTALLINE CROSPOVIDONE HYPROMELLOSE PHTHALATE (24% PHTHALATE, 55 CST) HYPROMELLOSES LACTOSE MONOHYDRATE SODIUM CHLORIDE SODIUM LAURYL SULFATE STARCH, CORN STEARIC ACID TALC TRIETHYL CITRATE WHITE TO OFF-WHITE OVAL 70;9 Doxycycline Hyclate Doxycycline Hyclate DOXYCYCLINE HYCLATE DOXYCYCLINE ANHYDROUS ANHYDROUS LACTOSE CELLULOSE, MICROCRYSTALLINE CROSPOVIDONE HYPROMELLOSE PHTHALATE (24% PHTHALATE, 55 CST) HYPROMELLOSES LACTOSE MONOHYDRATE SODIUM CHLORIDE SODIUM LAURYL SULFATE STARCH, CORN STEARIC ACID TALC TRIETHYL CITRATE WHITE TO OFF-WHITE CAPSULE 7;1;0

Application Number

ANDA206772

Brand Name

Doxycycline Hyclate

Generic Name

Doxycycline Hyclate

Product Ndc

70771-1589

Product Type

HUMAN PRESCRIPTION DRUG

Route

ORAL

Package Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1587-6 in bottle of 60 tablets Doxycycline Hyclate Delayed-release Tablets USP, 75 mg Rx only 60 tablets NDC 70771-1588-6 in bottle of 60 tablets Doxycycline Hyclate Delayed-release Tablets USP, 100 mg Rx only 60 tablets NDC 70771-1589-6 in bottle of 60 tablets Doxycycline Hyclate Delayed-release Tablets USP, 150 mg Rx only 60 tablets 75 mg label 100 mg label 150 mg label

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