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
- 24658-310_65cac0b6-3550-48cf-bffa-cf42443c2731
- Product NDC
- 24658-310
- Form
- TABLET, FILM COATED
- Composition / generic term
- Doxycycline Hyclate
- Labeler
- PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250307
- Source listing expiry
- 20261231
Source-listed ingredients
- DOXYCYCLINE HYCLATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (24658-310-01) · 24658-310-01
- 500 TABLET, FILM COATED in 1 BOTTLE (24658-310-05) · 24658-310-05
- 300 TABLET, FILM COATED in 1 BOTTLE (24658-310-07) · 24658-310-07
- 400 TABLET, FILM COATED in 1 BOTTLE (24658-310-08) · 24658-310-08
- 1000 TABLET, FILM COATED in 1 BOTTLE (24658-310-10) · 24658-310-10
- 20 TABLET, FILM COATED in 1 BOTTLE (24658-310-20) · 24658-310-20
- 210 TABLET, FILM COATED in 1 BOTTLE (24658-310-21) · 24658-310-21
- 30 TABLET, FILM COATED in 1 BOTTLE (24658-310-30) · 24658-310-30
- 50 TABLET, FILM COATED in 1 BOTTLE (24658-310-50) · 24658-310-50
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 →