NDC 0093-3421 – Cyclobenzaprine Hydrochloride

Cyclobenzaprine Hydrochloride 7.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0093-3421

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA071611
Marketed since
July 20, 2021
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0093-3421-01100 TABLET, FILM COATED in 1 BOTTLE (0093-3421-01)Jul 20, 2021

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