United States · FDA National Drug Code directory
Minocycline Hydrochloride
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
- 67877-577_51213aa1-873c-4b55-a36d-3ebbb73fa220
- Product NDC
- 67877-577
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Minocycline Hydrochloride
- Labeler
- Ascend Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160930
- Source listing expiry
- 20261231
Source-listed ingredients
- MINOCYCLINE HYDROCHLORIDE — 135 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-577-01) · 67877-577-01
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-577-05) · 67877-577-05
- 10 BLISTER PACK in 1 CARTON (67877-577-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK · 67877-577-14
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-577-30) · 67877-577-30
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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