Package 0093-8741-01

Brand: mexiletine hydrochloride

Generic: mexiletine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-8741-01
Digits Only 0093874101
Product NDC 0093-8741
Product ID 0093-8741_e7a9997c-4cf7-4cf1-94c0-ff60f15ae0f9
Description

100 CAPSULE in 1 BOTTLE (0093-8741-01)

Marketing

Marketing Status
Marketed Since 1995-06-05
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": "e7a9997c-4cf7-4cf1-94c0-ff60f15ae0f9", "openfda": {"upc": ["0300938741014", "0300938739011"], "unii": ["606D60IS38"], "rxcui": ["1362706", "1362712", "1362720"], "spl_set_id": ["693da40b-26d4-40d6-87d1-158e256f40ab"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0093-8741-01)", "package_ndc": "0093-8741-01", "marketing_start_date": "19950605"}], "brand_name": "Mexiletine Hydrochloride", "product_id": "0093-8741_e7a9997c-4cf7-4cf1-94c0-ff60f15ae0f9", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "0093-8741", "generic_name": "Mexiletine Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mexiletine Hydrochloride", "active_ingredients": [{"name": "MEXILETINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA074377", "marketing_category": "ANDA", "marketing_start_date": "19950605", "listing_expiration_date": "20261231"}