NDC 76420-269 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC76420-269

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA071611
Marketed since
July 20, 2021
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
76420-269-011 TABLET, FILM COATED in 1 BOTTLE (76420-269-01)Sep 3, 2022
76420-269-022 TABLET, FILM COATED in 1 BOTTLE (76420-269-02)Sep 3, 2022
76420-269-077 TABLET, FILM COATED in 1 BOTTLE (76420-269-07)Sep 3, 2022
76420-269-10100 TABLET, FILM COATED in 1 BOTTLE (76420-269-10)Sep 3, 2022
76420-269-1515 TABLET, FILM COATED in 1 BOTTLE (76420-269-15)Sep 3, 2022
76420-269-2020 TABLET, FILM COATED in 1 BOTTLE (76420-269-20)Sep 3, 2022
76420-269-3030 TABLET, FILM COATED in 1 BOTTLE (76420-269-30)Sep 3, 2022
76420-269-6060 TABLET, FILM COATED in 1 BOTTLE (76420-269-60)Sep 3, 2022
76420-269-9090 TABLET, FILM COATED in 1 BOTTLE (76420-269-90)Sep 3, 2022

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