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
- 68308-716_fe12dd75-ce55-4035-9193-0182bc4f5ba6
- Product NDC
- 68308-716
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Doxycycline Hyclate
- Labeler
- Mayne Pharma Commercial LLC
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20160201
- Source listing expiry
- 20261231
Source-listed ingredients
- DOXYCYCLINE HYCLATE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68308-716-30) · 68308-716-30
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68308-716-60) · 68308-716-60
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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