NDC 53489-647 – Doxycycline Hyclate

Doxycycline Hyclate 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC53489-647

Product details

Brand name
Doxycycline Hyclate
Generic name
Doxycycline Hyclate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA065134
Marketed since
May 13, 2005
Listing expires
December 31, 2026
Pharmacologic class
Tetracycline-class Drug

Active ingredients

Uses, dosage, side effects and warnings for Doxycycline Hyclate →

Package NDC codes (7)

Package NDCDescriptionSince
53489-647-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-01)May 13, 2005
53489-647-03250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-03)May 13, 2005
53489-647-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-05)May 13, 2005
53489-647-0660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-06)May 13, 2005
53489-647-0730 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-07)May 13, 2005
53489-647-101000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-10)May 13, 2005
53489-647-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-90)May 13, 2005

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