United States · FDA National Drug Code directory
Doxycycline
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 23155-135_ec6854e5-3f41-4b8f-be77-49e3bd19f7c4
- Product NDC
- 23155-135
- Form
- TABLET
- Composition / generic term
- Doxycycline
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120501
- Source listing expiry
- 20261231
Source-listed ingredients
- DOXYCYCLINE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BOTTLE (23155-135-05) · 23155-135-05
- 10 TABLET in 1 BLISTER PACK (23155-135-11) · 23155-135-11
- 50 TABLET in 1 BOTTLE (23155-135-25) · 23155-135-25
- 30 TABLET in 1 CARTON (23155-135-30) · 23155-135-30
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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