United States · FDA National Drug Code directory

Cyclobenzaprine Hydrochloride

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
72789-046_3403a5e2-c822-d823-e063-6394a90a7142
Product NDC
72789-046
Form
TABLET, FILM COATED
Composition / generic term
cyclobenzaprine hydrochloride
Labeler
PD-Rx Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20170330
Source listing expiry
20261231

Source-listed ingredients

  • CYCLOBENZAPRINE HYDROCHLORIDE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-03) · 72789-046-03
  • 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-04) · 72789-046-04
  • 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-06) · 72789-046-06
  • 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-10) · 72789-046-10
  • 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-12) · 72789-046-12
  • 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-14) · 72789-046-14
  • 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-20) · 72789-046-20
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-30) · 72789-046-30
  • 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-40) · 72789-046-40
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-60) · 72789-046-60

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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