NDC 76420-268 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC76420-268

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
76420-268-011 TABLET, FILM COATED in 1 BOTTLE (76420-268-01)Sep 3, 2022
76420-268-022 TABLET, FILM COATED in 1 BOTTLE (76420-268-02)Sep 3, 2022
76420-268-077 TABLET, FILM COATED in 1 BOTTLE (76420-268-07)Sep 3, 2022
76420-268-10100 TABLET, FILM COATED in 1 BOTTLE (76420-268-10)Sep 3, 2022
76420-268-1515 TABLET, FILM COATED in 1 BOTTLE (76420-268-15)Sep 3, 2022
76420-268-2020 TABLET, FILM COATED in 1 BOTTLE (76420-268-20)Sep 3, 2022
76420-268-3030 TABLET, FILM COATED in 1 BOTTLE (76420-268-30)Sep 3, 2022
76420-268-6060 TABLET, FILM COATED in 1 BOTTLE (76420-268-60)Sep 3, 2022
76420-268-9090 TABLET, FILM COATED in 1 BOTTLE (76420-268-90)Sep 3, 2022

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