Package 68071-4935-6

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4935-6
Digits Only 6807149356
Product NDC 68071-4935
Product ID 68071-4935_1ae26a9a-3bd7-c2fc-e063-6294a90a89bb
Description

6 TABLET, FILM COATED in 1 BOTTLE (68071-4935-6)

Marketing

Marketing Status
Marketed Since 2019-06-21
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": "1ae26a9a-3bd7-c2fc-e063-6294a90a89bb", "openfda": {"upc": ["0368071493566"], "unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["8bdc725e-22e3-0f32-e053-2a95a90ae8a9"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (68071-4935-6)", "package_ndc": "68071-4935-6", "marketing_start_date": "20190621"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "68071-4935_1ae26a9a-3bd7-c2fc-e063-6294a90a89bb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68071-4935", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20261231"}