United States · FDA National Drug Code directory
Tetracycline 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
- 82644-870_3d44a562-4fde-4867-90e6-433ea752bb3c
- Product NDC
- 82644-870
- Form
- TABLET, FILM COATED
- Composition / generic term
- Tetracycline Hydrochloride
- Labeler
- Pharmaka Generics Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240119
- Source listing expiry
- 20261231
Source-listed ingredients
- TETRACYCLINE HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED in 1 BOTTLE (82644-870-60) · 82644-870-60
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →