United States · FDA National Drug Code directory
PERAMPANEL
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
- 72205-071_4d8be129-f3cb-49ad-ae5a-a74a50dff689
- Product NDC
- 72205-071
- Form
- SUSPENSION
- Composition / generic term
- PERAMPANEL
- Labeler
- Novadoz Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250711
- Source listing expiry
- 20261231
Source-listed ingredients
- PERAMPANEL — .5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 340 mL in 1 BOTTLE (72205-071-79) · 72205-071-79
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 →