NDC 63304-132 – Doxycycline

Doxycycline 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC63304-132

Product details

Brand name
Doxycycline
Generic name
Doxycycline
Labeler
Sun Pharmaceutical Industries Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA065356
Marketed since
August 6, 2018
Listing expires
December 31, 2026
Pharmacologic class
Tetracycline-class Drug

Active ingredients

Uses, dosage, side effects and warnings for Doxycycline →

Package NDC codes (3)

Package NDCDescriptionSince
63304-132-04250 TABLET, FILM COATED in 1 BOTTLE (63304-132-04)Aug 6, 2018
63304-132-101000 TABLET, FILM COATED in 1 BOTTLE (63304-132-10)Aug 6, 2018
63304-132-5050 TABLET, FILM COATED in 1 BOTTLE (63304-132-50)Aug 6, 2018

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