NDC 50090-5756 – Cyclobenzaprine hydrochloride

Cyclobenzaprine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-5756

Product details

Brand name
Cyclobenzaprine hydrochloride
Generic name
Cyclobenzaprine hydrochloride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213324
Marketed since
July 6, 2020
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
50090-5756-030 TABLET, FILM COATED in 1 BOTTLE (50090-5756-0)Oct 1, 2021
50090-5756-120 TABLET, FILM COATED in 1 BOTTLE (50090-5756-1)Oct 1, 2021
50090-5756-290 TABLET, FILM COATED in 1 BOTTLE (50090-5756-2)Oct 1, 2021
50090-5756-324 TABLET, FILM COATED in 1 BOTTLE (50090-5756-3)Nov 1, 2021
50090-5756-410 TABLET, FILM COATED in 1 BOTTLE (50090-5756-4)May 17, 2024
50090-5756-57 TABLET, FILM COATED in 1 BOTTLE (50090-5756-5)Sep 22, 2026

Other Cyclobenzaprine Hydrochloride products