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
63629-1564_1a6afbdf-cba9-4ed0-9d82-1f47fb32dd7a
Product NDC
63629-1564
Form
TABLET, EXTENDED RELEASE
Composition / generic term
ORPHENADRINE CITRATE
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
19980619
Source listing expiry
20261231

Source-listed ingredients

  • ORPHENADRINE CITRATE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 56 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1564-0) · 63629-1564-0
  • 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1564-1) · 63629-1564-1
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1564-2) · 63629-1564-2
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1564-3) · 63629-1564-3
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1564-4) · 63629-1564-4
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1564-5) · 63629-1564-5
  • 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1564-6) · 63629-1564-6
  • 45 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1564-7) · 63629-1564-7
  • 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1564-8) · 63629-1564-8
  • 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1564-9) · 63629-1564-9

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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