NDC 70518-3251 – Cyclobenzaprine hydrochloride

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

Human Prescription Drug

Product NDC70518-3251

Product details

Brand name
Cyclobenzaprine hydrochloride
Generic name
Cyclobenzaprine hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213324
Marketed since
October 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 (3)

Package NDCDescriptionSince
70518-3251-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3251-1)Nov 16, 2021
70518-3251-230 TABLET, FILM COATED in 1 BLISTER PACK (70518-3251-2)Nov 23, 2021
70518-3251-615 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3251-6)Jun 9, 2025

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