NDC 70518-3474 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC70518-3474

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078643
Marketed since
August 9, 2022
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
70518-3474-25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-2)Aug 13, 2022
70518-3474-460 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-4)Aug 23, 2022
70518-3474-515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-5)Aug 23, 2022
70518-3474-720 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-7)Sep 29, 2022
70518-3474-890 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-8)Nov 9, 2022
70518-3474-930 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-9)Dec 1, 2022

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