NDC 68071-3150 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC68071-3150

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090478
Marketed since
July 22, 2016
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
68071-3150-121 TABLET, FILM COATED in 1 BOTTLE (68071-3150-1)Mar 7, 2017
68071-3150-220 TABLET, FILM COATED in 1 BOTTLE (68071-3150-2)Mar 7, 2017
68071-3150-330 TABLET, FILM COATED in 1 BOTTLE (68071-3150-3)Mar 7, 2017
68071-3150-484 TABLET, FILM COATED in 1 BOTTLE (68071-3150-4)Mar 16, 2017
68071-3150-515 TABLET, FILM COATED in 1 BOTTLE (68071-3150-5)Mar 7, 2017
68071-3150-660 TABLET, FILM COATED in 1 BOTTLE (68071-3150-6)Mar 7, 2017
68071-3150-77 TABLET, FILM COATED in 1 BOTTLE (68071-3150-7)Mar 7, 2017
68071-3150-86 TABLET, FILM COATED in 1 BOTTLE (68071-3150-8)Mar 7, 2017
68071-3150-990 TABLET, FILM COATED in 1 BOTTLE (68071-3150-9)Mar 7, 2017

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