United States · FDA National Drug Code directory
Clonazepam
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
- 71335-0333_782450b2-eb19-4b1d-8470-c43ce3de31f7
- Product NDC
- 71335-0333
- Form
- TABLET
- Composition / generic term
- clonazepam
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110603
- Source listing expiry
- 20261231
Source-listed ingredients
- CLONAZEPAM — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE, PLASTIC (71335-0333-1) · 71335-0333-1
- 60 TABLET in 1 BOTTLE, PLASTIC (71335-0333-2) · 71335-0333-2
- 90 TABLET in 1 BOTTLE, PLASTIC (71335-0333-3) · 71335-0333-3
- 120 TABLET in 1 BOTTLE, PLASTIC (71335-0333-4) · 71335-0333-4
- 10 TABLET in 1 BOTTLE, PLASTIC (71335-0333-5) · 71335-0333-5
- 180 TABLET in 1 BOTTLE, PLASTIC (71335-0333-6) · 71335-0333-6
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 →