Package 72603-310-02

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72603-310-02
Digits Only 7260331002
Product NDC 72603-310
Product ID 72603-310_4764d2fb-f80d-1435-e063-6294a90acd0b
Description

500 TABLET, FILM COATED in 1 BOTTLE (72603-310-02)

Marketing

Marketing Status
Marketed Since 2024-11-01
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cyclobenzaprine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4764d2fb-f80d-1435-e063-6294a90acd0b", "openfda": {"upc": ["0372603310023", "0372603312027", "0372603312034", "0372603311013", "0372603310016"], "unii": ["0VE05JYS2P"], "rxcui": ["828299", "828320", "828348"], "spl_set_id": ["2a3a13c3-116c-4e9e-a7f3-7ad7c80486c3"], "manufacturer_name": ["NORTHSTAR RX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72603-310-01)", "package_ndc": "72603-310-01", "marketing_start_date": "20241101"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72603-310-02)", "package_ndc": "72603-310-02", "marketing_start_date": "20241101"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "72603-310_4764d2fb-f80d-1435-e063-6294a90acd0b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72603-310", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "NORTHSTAR RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20271231"}