NDC 68071-2471 – Cyclobenzaprine hydrochloride

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

Human Prescription Drug

Product NDC68071-2471

Product details

Brand name
Cyclobenzaprine hydrochloride
Generic name
Cyclobenzaprine hydrochloride
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213324
Marketed since
July 6, 2020
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
68071-2471-115 TABLET, FILM COATED in 1 BOTTLE (68071-2471-1)Jul 7, 2021
68071-2471-220 TABLET, FILM COATED in 1 BOTTLE (68071-2471-2)Jul 7, 2021
68071-2471-721 TABLET, FILM COATED in 1 BOTTLE (68071-2471-7)Mar 11, 2024
68071-2471-990 TABLET, FILM COATED in 1 BOTTLE (68071-2471-9)Jul 7, 2021

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