Package 29300-414-01

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 29300-414-01
Digits Only 2930041401
Product NDC 29300-414
Description

100 TABLET, FILM COATED in 1 BOTTLE (29300-414-01)

Marketing

Marketing Status
Marketed Since 2020-09-30
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cc113cd6-8904-4485-b1b2-15dd5ff7468b", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299", "828320", "828348"], "spl_set_id": ["1adcdd8a-30f9-4a7b-853c-948a5589acab"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (29300-414-01)", "package_ndc": "29300-414-01", "marketing_start_date": "20200930"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (29300-414-10)", "package_ndc": "29300-414-10", "marketing_start_date": "20200930"}], "brand_name": "Cyclobenzaprine hydrochloride", "product_id": "29300-414_cc113cd6-8904-4485-b1b2-15dd5ff7468b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "29300-414", "generic_name": "Cyclobenzaprine hydrochloride", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA213324", "marketing_category": "ANDA", "marketing_start_date": "20200706", "listing_expiration_date": "20261231"}