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
- 70518-3869_5a6afbf5-95de-515f-e063-6294a90afa9c
- Product NDC
- 70518-3869
- Form
- TABLET
- Composition / generic term
- DOXYCYCLINE HYCLATE
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230924
- 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, PLASTIC (70518-3869-0) · 70518-3869-0
- 14 TABLET in 1 BOTTLE, PLASTIC (70518-3869-2) · 70518-3869-2
- 60 TABLET in 1 BOTTLE, PLASTIC (70518-3869-4) · 70518-3869-4
- 28 TABLET in 1 BOTTLE, PLASTIC (70518-3869-6) · 70518-3869-6
- 50 TABLET in 1 BOTTLE, PLASTIC (70518-3869-7) · 70518-3869-7
- 56 TABLET in 1 BOTTLE, PLASTIC (70518-3869-8) · 70518-3869-8
- 30 TABLET in 1 BLISTER PACK (70518-3869-9) · 70518-3869-9
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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