NDC 76420-839 – Cyclobenzaprine hydrochloride

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

Human Prescription Drug

Product NDC76420-839

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
76420-839-001000 TABLET, FILM COATED in 1 BOTTLE (76420-839-00)Aug 16, 2024
76420-839-011 TABLET, FILM COATED in 1 BOTTLE (76420-839-01)Aug 16, 2024
76420-839-022 TABLET, FILM COATED in 1 BOTTLE (76420-839-02)Aug 16, 2024
76420-839-05500 TABLET, FILM COATED in 1 BOTTLE (76420-839-05)Aug 16, 2024
76420-839-077 TABLET, FILM COATED in 1 BOTTLE (76420-839-07)Aug 16, 2024
76420-839-10100 TABLET, FILM COATED in 1 BOTTLE (76420-839-10)Aug 16, 2024
76420-839-2020 TABLET, FILM COATED in 1 BOTTLE (76420-839-20)Aug 16, 2024
76420-839-3030 TABLET, FILM COATED in 1 BOTTLE (76420-839-30)Aug 16, 2024
76420-839-6060 TABLET, FILM COATED in 1 BOTTLE (76420-839-60)Aug 16, 2024
76420-839-9090 TABLET, FILM COATED in 1 BOTTLE (76420-839-90)Aug 16, 2024

Other Cyclobenzaprine Hydrochloride products