Package 70512-872-10

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70512-872-10
Digits Only 7051287210
Product NDC 70512-872
Product ID 70512-872_3b2ac0d1-9247-b044-e063-6294a90a6780
Description

100 TABLET, FILM COATED in 1 BOTTLE (70512-872-10)

Marketing

Marketing Status
Marketed Since 2025-07-31
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": "3b2ac0d1-9247-b044-e063-6294a90a6780", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["db930d05-3f92-41f1-888c-301b2c4565e6"], "manufacturer_name": ["SOLA Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70512-872-10)", "package_ndc": "70512-872-10", "marketing_start_date": "20250731"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "70512-872_3b2ac0d1-9247-b044-e063-6294a90a6780", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70512-872", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "SOLA Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077563", "marketing_category": "ANDA", "marketing_start_date": "20250731", "listing_expiration_date": "20261231"}