Package 68071-3805-7

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3805-7
Digits Only 6807138057
Product NDC 68071-3805
Product ID 68071-3805_316e6fee-f10a-35f9-e063-6394a90a77ac
Description

21 TABLET, FILM COATED in 1 BOTTLE (68071-3805-7)

Marketing

Marketing Status
Marketed Since 2025-03-04
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": "316e6fee-f10a-35f9-e063-6394a90a77ac", "openfda": {"upc": ["0368071380576"], "unii": ["0VE05JYS2P"], "rxcui": ["828299"], "spl_set_id": ["2f89c8f6-7f3c-8396-e063-6294a90a643e"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (68071-3805-1)", "package_ndc": "68071-3805-1", "marketing_start_date": "20250304"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (68071-3805-7)", "package_ndc": "68071-3805-7", "marketing_start_date": "20250304"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "68071-3805_316e6fee-f10a-35f9-e063-6394a90a77ac", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68071-3805", "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": "7.5 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20261231"}