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: 62332-388_23a5f41d-9033-4744-9ac4-e2e3fe39e6b5
Product NDC: 62332-388
Form: TABLET, FILM COATED
Composition / generic term: DOXYCYCLINE HYCLATE
Labeler: Alembic Pharmaceuticals Inc.
Marketing category: ANDA
Marketing start / end (source format): 20200630
Source listing expiry: 20261231

Source-listed ingredients

DOXYCYCLINE HYCLATE — 150 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

60 TABLET, FILM COATED in 1 BOTTLE (62332-388-60) · 62332-388-60
1000 TABLET, FILM COATED in 1 BOTTLE (62332-388-91) · 62332-388-91

Source and coverage

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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.

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