Package 69306-015-03

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69306-015-03
Digits Only 6930601503
Product NDC 69306-015
Product ID 69306-015_3df3e06d-9fe0-2b90-e063-6294a90ab5af
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69306-015-03)

Marketing

Marketing Status
Marketed Since 2025-09-04
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": "3df3e06d-9fe0-2b90-e063-6294a90ab5af", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828358"], "spl_set_id": ["d4457b8c-fff8-4c19-8d5a-a667161e5446"], "manufacturer_name": ["Doc Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69306-015-03)", "package_ndc": "69306-015-03", "marketing_start_date": "20250904"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "69306-015_3df3e06d-9fe0-2b90-e063-6294a90ab5af", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "69306-015", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Doc Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "NDA021777", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190304", "listing_expiration_date": "20261231"}