Package 72189-101-60

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-101-60
Digits Only 7218910160
Product NDC 72189-101
Product ID 72189-101_2be875a1-0e9c-2e2a-e063-6394a90a1520
Description

60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-101-60)

Marketing

Marketing Status
Marketed Since 2020-05-07
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": "2be875a1-0e9c-2e2a-e063-6394a90a1520", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828358"], "spl_set_id": ["a512d34c-8164-0c04-e053-2995a90a1942"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-101-60)", "package_ndc": "72189-101-60", "marketing_start_date": "20200507"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "72189-101_2be875a1-0e9c-2e2a-e063-6394a90a1520", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72189-101", "generic_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA091281", "marketing_category": "ANDA", "marketing_start_date": "20200507", "listing_expiration_date": "20261231"}