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
- 46708-387_8becf01f-63de-4cf3-881e-94d18fe9274c
- Product NDC
- 46708-387
- Form
- TABLET, FILM COATED
- Composition / generic term
- DOXYCYCLINE HYCLATE
- Labeler
- Alembic Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200630
- Source listing expiry
- 20261231
Source-listed ingredients
- DOXYCYCLINE HYCLATE — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED in 1 BOTTLE (46708-387-60) · 46708-387-60
- 1000 TABLET, FILM COATED in 1 BOTTLE (46708-387-91) · 46708-387-91
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 →