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
33342-392_2696f799-7902-4239-807a-9ae85a5d0f1d
Product NDC
33342-392
Form
TABLET
Composition / generic term
Doxycycline Hyclate
Labeler
Macleods Pharmaceuticals Limited
Marketing category
ANDA
Marketing start / end (source format)
20251119
Source listing expiry
20271231

Source-listed ingredients

  • DOXYCYCLINE HYCLATE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 20 TABLET in 1 BOTTLE (33342-392-05) · 33342-392-05
  • 50 TABLET in 1 BOTTLE (33342-392-08) · 33342-392-08
  • 100 TABLET in 1 BOTTLE (33342-392-11) · 33342-392-11
  • 10 BLISTER PACK in 1 CARTON (33342-392-12) / 10 TABLET in 1 BLISTER PACK · 33342-392-12
  • 500 TABLET in 1 BOTTLE (33342-392-15) · 33342-392-15

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 →