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
- 72789-309_38052f8d-1d68-b250-e063-6394a90a8b48
- Product NDC
- 72789-309
- Form
- TABLET, FILM COATED
- Composition / generic term
- Doxycycline Hyclate
- Labeler
- PD-Rx Pharmaceuticals, 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 (72789-309-01) · 72789-309-01
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-309-60) · 72789-309-60
- 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-309-93) · 72789-309-93
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 →