United States · FDA National Drug Code directory
doxycycline
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
- 65841-822_d9de3252-a876-482e-be60-0a47eb985aa8
- Product NDC
- 65841-822
- Form
- CAPSULE
- Composition / generic term
- doxycycline
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160314
- Source listing expiry
- 20261231
Source-listed ingredients
- DOXYCYCLINE — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (65841-822-01) · 65841-822-01
- 500 CAPSULE in 1 BOTTLE (65841-822-05) · 65841-822-05
- 30 CAPSULE in 1 BOTTLE (65841-822-06) · 65841-822-06
- 1000 CAPSULE in 1 BOTTLE (65841-822-10) · 65841-822-10
- 90 CAPSULE in 1 BOTTLE (65841-822-16) · 65841-822-16
- 50 CAPSULE in 1 BOTTLE (65841-822-18) · 65841-822-18
- 10 BLISTER PACK in 1 CARTON (65841-822-77) / 10 CAPSULE in 1 BLISTER PACK (65841-822-30) · 65841-822-77
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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