Package 72789-156-15

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-156-15
Digits Only 7278915615
Product NDC 72789-156
Product ID 72789-156_34173b65-9a3a-f37a-e063-6394a90a0029
Description

15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-156-15)

Marketing

Marketing Status
Marketed Since 2021-01-12
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": "34173b65-9a3a-f37a-e063-6394a90a0029", "openfda": {"upc": ["0372789156156"], "unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["9161cb5e-63e5-41d7-9bde-66c7b7b7a2f3"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-156-15)", "package_ndc": "72789-156-15", "marketing_start_date": "20210112"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "72789-156_34173b65-9a3a-f37a-e063-6394a90a0029", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72789-156", "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": "10 mg/1"}], "application_number": "ANDA077797", "marketing_category": "ANDA", "marketing_start_date": "20170330", "listing_expiration_date": "20261231"}