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
- 68382-782_9486a93f-bc2a-444a-a8d4-3bce410d21c7
- Product NDC
- 68382-782
- Form
- CAPSULE
- Composition / generic term
- doxycycline
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160314
- Source listing expiry
- 20261231
Source-listed ingredients
- DOXYCYCLINE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (68382-782-01) · 68382-782-01
- 500 CAPSULE in 1 BOTTLE (68382-782-05) · 68382-782-05
- 30 CAPSULE in 1 BOTTLE (68382-782-06) · 68382-782-06
- 1000 CAPSULE in 1 BOTTLE (68382-782-10) · 68382-782-10
- 90 CAPSULE in 1 BOTTLE (68382-782-16) · 68382-782-16
- 50 CAPSULE in 1 BOTTLE (68382-782-18) · 68382-782-18
- 10 BLISTER PACK in 1 CARTON (68382-782-77) / 10 CAPSULE in 1 BLISTER PACK (68382-782-30) · 68382-782-77
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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