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
68071-4836_1ae175c6-5f09-8a7a-e063-6294a90a6461
Product NDC
68071-4836
Form
TABLET, FILM COATED
Composition / generic term
Doxycycline Hyclate
Labeler
NuCare Pharmaceuticals,Inc.
Marketing category
ANDA
Marketing start / end (source format)
20161001
Source listing expiry
20261231

Source-listed ingredients

  • DOXYCYCLINE HYCLATE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 TABLET, FILM COATED in 1 BOTTLE (68071-4836-1) · 68071-4836-1
  • 14 TABLET, FILM COATED in 1 BOTTLE (68071-4836-7) · 68071-4836-7
  • 28 TABLET, FILM COATED in 1 BOTTLE (68071-4836-8) · 68071-4836-8

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 →