Package 69306-872-03

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69306-872-03
Digits Only 6930687203
Product NDC 69306-872
Product ID 69306-872_426ec634-b00d-e57d-e063-6394a90a4103
Description

30 TABLET, FILM COATED in 1 BOTTLE (69306-872-03)

Marketing

Marketing Status
Marketed Since 2025-10-31
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": "426ec634-b00d-e57d-e063-6394a90a4103", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["4c054230-1978-44d2-9467-ed1994619113"], "manufacturer_name": ["Doc Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (69306-872-03)", "package_ndc": "69306-872-03", "marketing_start_date": "20251031"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (69306-872-06)", "package_ndc": "69306-872-06", "marketing_start_date": "20251031"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "69306-872_426ec634-b00d-e57d-e063-6394a90a4103", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "69306-872", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Doc Rx", "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"}