NDC 63304-173 – Doxycycline

Doxycycline 150 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC63304-173

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 (4)

Package NDCDescriptionSince
63304-173-0310 TABLET, FILM COATED in 1 BOTTLE (63304-173-03)Aug 6, 2018
63304-173-101000 TABLET, FILM COATED in 1 BOTTLE (63304-173-10)Aug 6, 2018
63304-173-3030 TABLET, FILM COATED in 1 BOTTLE (63304-173-30)Aug 6, 2018
63304-173-691 BLISTER PACK in 1 CARTON (63304-173-69) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-173-11)Aug 6, 2018

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