NDC 76420-841 – Cyclobenzaprine hydrochloride

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

Human Prescription Drug

Product NDC76420-841

Product details

Brand name
Cyclobenzaprine hydrochloride
Generic name
Cyclobenzaprine hydrochloride
Labeler
Asclemed USA, 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 (10)

Package NDCDescriptionSince
76420-841-001000 TABLET, FILM COATED in 1 BOTTLE (76420-841-00)Aug 16, 2024
76420-841-011 TABLET, FILM COATED in 1 BOTTLE (76420-841-01)Aug 16, 2024
76420-841-022 TABLET, FILM COATED in 1 BOTTLE (76420-841-02)Aug 16, 2024
76420-841-05500 TABLET, FILM COATED in 1 BOTTLE (76420-841-05)Aug 16, 2024
76420-841-077 TABLET, FILM COATED in 1 BOTTLE (76420-841-07)Aug 16, 2024
76420-841-10100 TABLET, FILM COATED in 1 BOTTLE (76420-841-10)Aug 16, 2024
76420-841-2020 TABLET, FILM COATED in 1 BOTTLE (76420-841-20)Aug 16, 2024
76420-841-3030 TABLET, FILM COATED in 1 BOTTLE (76420-841-30)Aug 16, 2024
76420-841-6060 TABLET, FILM COATED in 1 BOTTLE (76420-841-60)Aug 16, 2024
76420-841-9090 TABLET, FILM COATED in 1 BOTTLE (76420-841-90)Aug 16, 2024

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