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
- 70771-1359_cb5b26e1-ae6e-46a2-9edd-e3e98ced7a6d
- Product NDC
- 70771-1359
- Form
- CAPSULE
- Composition / generic term
- Doxycycline hyclate
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180912
- Source listing expiry
- 20261231
Source-listed ingredients
- DOXYCYCLINE HYCLATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 CAPSULE in 1 BOTTLE (70771-1359-0) · 70771-1359-0
- 100 CAPSULE in 1 BOTTLE (70771-1359-1) · 70771-1359-1
- 10 BLISTER PACK in 1 CARTON (70771-1359-4) / 10 CAPSULE in 1 BLISTER PACK (70771-1359-2) · 70771-1359-4
- 500 CAPSULE in 1 BOTTLE (70771-1359-5) · 70771-1359-5
- 50 CAPSULE in 1 BOTTLE (70771-1359-7) · 70771-1359-7
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →