NDC 70518-3702 – Cyclobenzaprine hydrochloride

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

Human Prescription Drug

Product NDC70518-3702

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
April 6, 2023
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
70518-3702-130 TABLET, FILM COATED in 1 BLISTER PACK (70518-3702-1)Apr 12, 2023
70518-3702-330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3702-3)May 4, 2024

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