NDC 72189-080 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC72189-080

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
DIRECT RX
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208170
Marketed since
May 13, 2020
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
72189-080-077 TABLET, FILM COATED in 1 BOTTLE (72189-080-07)May 13, 2020
72189-080-1010 TABLET, FILM COATED in 1 BOTTLE (72189-080-10)May 13, 2020
72189-080-1515 TABLET, FILM COATED in 1 BOTTLE (72189-080-15)May 13, 2020
72189-080-2020 TABLET, FILM COATED in 1 BOTTLE (72189-080-20)May 13, 2020
72189-080-2121 TABLET, FILM COATED in 1 BOTTLE (72189-080-21)May 13, 2020
72189-080-3030 TABLET, FILM COATED in 1 BOTTLE (72189-080-30)May 13, 2020
72189-080-4545 TABLET, FILM COATED in 1 BOTTLE (72189-080-45)May 13, 2020
72189-080-6060 TABLET, FILM COATED in 1 BOTTLE (72189-080-60)May 13, 2020
72189-080-72120 TABLET, FILM COATED in 1 BOTTLE (72189-080-72)May 13, 2020
72189-080-9090 TABLET, FILM COATED in 1 BOTTLE (72189-080-90)May 13, 2020

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