DOXYCYCLINE tablet, film coated

Doxycycline by

Drug Labeling and Warnings

Doxycycline by is a Prescription medication manufactured, distributed, or labeled by Blessings International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL - 100 mg Tablet Bottle Label

BLESSINGS
INTERNATIONAL®
MEDICINESFORMISSIONS

NDC: 51376-780-10

Doxycycline

100 mg

1,000 Film Coated Tablets USP

RX ONLY / FOR EXPORT ONLY

INGREDIENTS AND APPEARANCE

DOXYCYCLINE 
doxycycline tablet, film coated

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 51376-780
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Doxycycline (UNII: N12000U13O) (DOXYCYCLINE ANHYDROUS - UNII:334895S862)	DOXYCYCLINE ANHYDROUS	100 mg

Inactive Ingredients
Ingredient Name	Strength
Magnesium Stearate (UNII: 70097M6I30)
Isopropyl Alcohol (UNII: ND2M416302)
Methylene Chloride (UNII: 588X2YUY0A)
Microcrystalline Cellulose (UNII: OP1R32D61U)
Talc (UNII: 7SEV7J4R1U)
Starch, Potato (UNII: 8I089SAH3T)

Product Characteristics
Color	ORANGE	Score	no score
Shape	ROUND	Size	10mm
Flavor		Imprint Code	DOXYC
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51376-780-10	1000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2008

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Export only		05/01/2008

Labeler - Blessings International (064965742)

Establishment
Name	Address	ID/FEI	Business Operations
Blessings International		064965742	MANUFACTURE(51376-780)