United States · FDA National Drug Code directory

Orphenadrine Citrate

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
49999-046_018c5bb2-b5ea-4e62-8670-3e099c32ead9
Product NDC
49999-046
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Orphenadrine Citrate
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Marketing category
ANDA
Marketing start / end (source format)
20110207 / 20261130

Source-listed ingredients

  • ORPHENADRINE CITRATE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49999-046-60) · 49999-046-60

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 →