Package 72789-073-30

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-073-30
Digits Only 7278907330
Product NDC 72789-073
Product ID 72789-073_340442be-1fd5-2781-e063-6294a90a4f8c
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-073-30)

Marketing

Marketing Status
Marketed Since 2020-04-08
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": "340442be-1fd5-2781-e063-6294a90a4f8c", "openfda": {"upc": ["0372789073309"], "unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["3baeda95-d098-437a-b360-87a9c3f3fd9b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-073-30)", "package_ndc": "72789-073-30", "marketing_start_date": "20200408"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "72789-073_340442be-1fd5-2781-e063-6294a90a4f8c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72789-073", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA077797", "marketing_category": "ANDA", "marketing_start_date": "20170330", "listing_expiration_date": "20261231"}