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
- 43547-325_49c9be01-a1bf-48aa-8ef4-0584e8dcaac5
- Product NDC
- 43547-325
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- DOXYCYCLINE HYCLATE
- Labeler
- Solco Healthcare US LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161128
- Source listing expiry
- 20271231
Source-listed ingredients
- DOXYCYCLINE HYCLATE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE (43547-325-06) · 43547-325-06
- 100 TABLET, DELAYED RELEASE in 1 BOTTLE (43547-325-10) · 43547-325-10
- 500 TABLET, DELAYED RELEASE in 1 BOTTLE (43547-325-50) · 43547-325-50
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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