Package 55700-239-90

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55700-239-90
Digits Only 5570023990
Product NDC 55700-239
Product ID 55700-239_0498b9cc-1111-40b9-9605-08c32d167c7f
Description

90 TABLET, FILM COATED in 1 BOTTLE (55700-239-90)

Marketing

Marketing Status
Discontinued 2027-12-31
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": "0498b9cc-1111-40b9-9605-08c32d167c7f", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299"], "spl_set_id": ["794d350b-6c88-41d5-b68b-3e2c57ee2a4f"], "manufacturer_name": ["Quality Care Products LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (55700-239-90)", "package_ndc": "55700-239-90", "marketing_end_date": "20271231", "marketing_start_date": "20220408"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "55700-239_0498b9cc-1111-40b9-9605-08c32d167c7f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "55700-239", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Quality Care Products LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA078722", "marketing_category": "ANDA", "marketing_end_date": "20271231", "marketing_start_date": "20150325"}