United States · FDA National Drug Code directory
Demeclocycline Hydrochloride
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
- 53746-555_04625dca-8f81-4c33-acd2-c8c2693f8483
- Product NDC
- 53746-555
- Form
- TABLET
- Composition / generic term
- Demeclocycline
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220525
- Source listing expiry
- 20271231
Source-listed ingredients
- DEMECLOCYCLINE HYDROCHLORIDE — 300 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 48 TABLET in 1 BOTTLE (53746-555-48) · 53746-555-48
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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