NDC 68071-3567 – Cyclobenzaprine hydrochloride

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

Human Prescription Drug

Product NDC68071-3567

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, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
68071-3567-020 TABLET, FILM COATED in 1 BOTTLE (68071-3567-0)Jun 23, 2026
68071-3567-212 TABLET, FILM COATED in 1 BOTTLE (68071-3567-2)Feb 2, 2024
68071-3567-330 TABLET, FILM COATED in 1 BOTTLE (68071-3567-3)Feb 2, 2024

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