United States · FDA National Drug Code directory
Doxycycline Hyclate
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
- 53489-647_31dd6775-5a9a-9e21-e063-6294a90aa546
- Product NDC
- 53489-647
- Form
- TABLET, FILM COATED
- Composition / generic term
- Doxycycline Hyclate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20050513
- Source listing expiry
- 20261231
Source-listed ingredients
- DOXYCYCLINE HYCLATE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-01) · 53489-647-01
- 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-03) · 53489-647-03
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-05) · 53489-647-05
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-06) · 53489-647-06
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-07) · 53489-647-07
- 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-10) · 53489-647-10
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-90) · 53489-647-90
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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