United States · FDA National Drug Code directory
Felbamate
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
- 16714-775_c3010d7b-f928-464e-af7c-ca45a5320a20
- Product NDC
- 16714-775
- Form
- SUSPENSION
- Composition / generic term
- Felbamate
- Labeler
- NORTHSTAR RX LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180410
- Source listing expiry
- 20261231
Source-listed ingredients
- FELBAMATE — 600 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 237 mL in 1 BOTTLE (16714-775-01) · 16714-775-01
- 473 mL in 1 BOTTLE (16714-775-02) · 16714-775-02
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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