NDC 63187-812 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC63187-812

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090478
Marketed since
July 22, 2016
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (11)

Package NDCDescriptionSince
63187-812-077 TABLET, FILM COATED in 1 BOTTLE (63187-812-07)May 14, 2021
63187-812-1010 TABLET, FILM COATED in 1 BOTTLE (63187-812-10)Aug 1, 2017
63187-812-1212 TABLET, FILM COATED in 1 BOTTLE (63187-812-12)Apr 2, 2018
63187-812-1515 TABLET, FILM COATED in 1 BOTTLE (63187-812-15)Feb 2, 2017
63187-812-2020 TABLET, FILM COATED in 1 BOTTLE (63187-812-20)Feb 2, 2017
63187-812-2121 TABLET, FILM COATED in 1 BOTTLE (63187-812-21)Feb 1, 2017
63187-812-3030 TABLET, FILM COATED in 1 BOTTLE (63187-812-30)Feb 1, 2017
63187-812-4545 TABLET, FILM COATED in 1 BOTTLE (63187-812-45)Feb 1, 2017
63187-812-6060 TABLET, FILM COATED in 1 BOTTLE (63187-812-60)Feb 1, 2017
63187-812-72120 TABLET, FILM COATED in 1 BOTTLE (63187-812-72)Feb 1, 2018
63187-812-9090 TABLET, FILM COATED in 1 BOTTLE (63187-812-90)Feb 1, 2017

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