Package 68071-3915-2

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3915-2
Digits Only 6807139152
Product NDC 68071-3915
Product ID 68071-3915_4511ceb6-8ad3-20d4-e063-6394a90ae4d5
Description

12 TABLET, FILM COATED in 1 BOTTLE (68071-3915-2)

Marketing

Marketing Status
Marketed Since 2025-11-17
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": "4511ceb6-8ad3-20d4-e063-6394a90ae4d5", "openfda": {"upc": ["0368071391527"], "unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["43ce2c79-ec4a-5120-e063-6394a90af6e1"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE (68071-3915-2)", "package_ndc": "68071-3915-2", "marketing_start_date": "20251117"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3915-3)", "package_ndc": "68071-3915-3", "marketing_start_date": "20251203"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "68071-3915_4511ceb6-8ad3-20d4-e063-6394a90ae4d5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68071-3915", "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": "5 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20261231"}