Package 52817-330-50

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 52817-330-50
Digits Only 5281733050
Product NDC 52817-330
Product ID 52817-330_b8c3dbd2-89f7-215b-e053-2995a90a7f74
Description

500 TABLET, FILM COATED in 1 BOTTLE (52817-330-50)

Marketing

Marketing Status
Marketed Since 2017-05-31
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": "b8c3dbd2-89f7-215b-e053-2995a90a7f74", "openfda": {"upc": ["0352817332103", "0352817330109", "0352817332004", "0352817331106", "0352817330505", "0352817332509"], "unii": ["0VE05JYS2P"], "rxcui": ["828299", "828320", "828348"], "spl_set_id": ["08adc97f-feef-46fb-ac75-f015b4f3a43a"], "manufacturer_name": ["TruPharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (52817-330-10)", "package_ndc": "52817-330-10", "marketing_start_date": "20170531"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (52817-330-50)", "package_ndc": "52817-330-50", "marketing_start_date": "20170531"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "52817-330_b8c3dbd2-89f7-215b-e053-2995a90a7f74", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "52817-330", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "TruPharma LLC", "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"}