NDC 10702-006 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC10702-006

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
KVK-TECH, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078048
Marketed since
July 31, 2014
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
10702-006-01100 TABLET, FILM COATED in 1 BOTTLE (10702-006-01)Jul 31, 2014
10702-006-101000 TABLET, FILM COATED in 1 BOTTLE (10702-006-10)Jul 31, 2014
10702-006-50500 TABLET, FILM COATED in 1 BOTTLE (10702-006-50)Jul 31, 2014

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