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
- 43547-462_49c9be01-a1bf-48aa-8ef4-0584e8dcaac5
- Product NDC
- 43547-462
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- DOXYCYCLINE HYCLATE
- Labeler
- Solco Healthcare US LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181128
- Source listing expiry
- 20271231
Source-listed ingredients
- DOXYCYCLINE HYCLATE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET, DELAYED RELEASE in 1 BOTTLE (43547-462-12) · 43547-462-12
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 →