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
- 71335-2113_2a8fc1ec-e0ab-4418-ac20-93d68fa4a5fc
- Product NDC
- 71335-2113
- Form
- TABLET
- Composition / generic term
- Doxycycline Hyclate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190314
- Source listing expiry
- 20261231
Source-listed ingredients
- DOXYCYCLINE HYCLATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET in 1 BOTTLE (71335-2113-1) · 71335-2113-1
- 30 TABLET in 1 BOTTLE (71335-2113-2) · 71335-2113-2
- 50 TABLET in 1 BOTTLE (71335-2113-3) · 71335-2113-3
- 14 TABLET in 1 BOTTLE (71335-2113-4) · 71335-2113-4
- 40 TABLET in 1 BOTTLE (71335-2113-5) · 71335-2113-5
- 60 TABLET in 1 BOTTLE (71335-2113-6) · 71335-2113-6
- 28 TABLET in 1 BOTTLE (71335-2113-7) · 71335-2113-7
- 10 TABLET in 1 BOTTLE (71335-2113-8) · 71335-2113-8
- 6 TABLET in 1 BOTTLE (71335-2113-9) · 71335-2113-9
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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