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
- 72789-319_570c33a6-761e-f46b-e063-6294a90a7862
- Product NDC
- 72789-319
- Form
- TABLET, FILM COATED
- Composition / generic term
- Doxycycline Hyclate
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19860710
- Source listing expiry
- 20271231
Source-listed ingredients
- DOXYCYCLINE HYCLATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-06) · 72789-319-06
- 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-07) · 72789-319-07
- 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-10) · 72789-319-10
- 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-14) · 72789-319-14
- 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-28) · 72789-319-28
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-30) · 72789-319-30
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-60) · 72789-319-60
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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