NDC 72789-046 – Cyclobenzaprine Hydrochloride

Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72789-046

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine hydrochloride
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077797
Marketed since
March 30, 2017
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →

Package NDC codes (10)

Package NDCDescriptionSince
72789-046-033 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-03)Jan 7, 2020
72789-046-044 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-04)Jan 6, 2020
72789-046-066 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-06)Jul 17, 2020
72789-046-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-10)Jan 8, 2020
72789-046-1212 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-12)Jun 15, 2020
72789-046-1414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-14)Jan 27, 2020
72789-046-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-20)Jan 6, 2020
72789-046-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-30)Jan 6, 2020
72789-046-4040 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-40)Jun 1, 2020
72789-046-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-60)Jan 6, 2020

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