Package 31722-038-01

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 31722-038-01
Digits Only 3172203801
Product NDC 31722-038
Product ID 31722-038_ed93311a-2bfc-3875-e053-2a95a90ac6f0
Description

100 CAPSULE in 1 BOTTLE (31722-038-01)

Marketing

Marketing Status
Marketed Since 2022-11-09
Brand mexiletine hydrochloride
Generic mexiletine hydrochloride
Sample Package No

Linked Drug Pages (1)

Mexiletine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ed93311a-2bfc-3875-e053-2a95a90ac6f0", "openfda": {"upc": ["0331722036016", "0331722037013", "0331722038010"], "unii": ["606D60IS38"], "rxcui": ["1362706", "1362712", "1362720"], "spl_set_id": ["8b20e850-037b-4c16-a57d-c3d4909f147a"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (31722-038-01)", "package_ndc": "31722-038-01", "marketing_start_date": "20221109"}], "brand_name": "Mexiletine hydrochloride", "product_id": "31722-038_ed93311a-2bfc-3875-e053-2a95a90ac6f0", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "31722-038", "generic_name": "Mexiletine hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mexiletine hydrochloride", "active_ingredients": [{"name": "MEXILETINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA216463", "marketing_category": "ANDA", "marketing_start_date": "20221109", "listing_expiration_date": "20261231"}