NDC 23155-135 – Doxycycline

Doxycycline 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC23155-135

Product details

Brand name
Doxycycline
Generic name
Doxycycline
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091605
Marketed since
May 1, 2012
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
23155-135-05500 TABLET in 1 BOTTLE (23155-135-05)May 1, 2012
23155-135-1110 TABLET in 1 BLISTER PACK (23155-135-11)May 1, 2012
23155-135-2550 TABLET in 1 BOTTLE (23155-135-25)May 1, 2012
23155-135-3030 TABLET in 1 CARTON (23155-135-30)May 1, 2012

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