Package 82982-027-30

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82982-027-30
Digits Only 8298202730
Product NDC 82982-027
Description

30 TABLET, FILM COATED in 1 BOTTLE (82982-027-30)

Marketing

Marketing Status
Discontinued 2026-03-31
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "198ca554-e360-5da4-e063-6294a90adf71", "openfda": {"upc": ["0382982027306"], "unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["f5633c0d-bcf3-b9f6-e053-2a95a90a9353"], "manufacturer_name": ["Pharmasource Meds, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82982-027-30)", "package_ndc": "82982-027-30", "marketing_end_date": "20260331", "marketing_start_date": "20230308"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "82982-027_198ca554-e360-5da4-e063-6294a90adf71", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "82982-027", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "Pharmasource Meds, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077797", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20230308"}