mexiletine hydrochloride
Generic: mexiletine hydrochloride
Labeler: golden state medical supply, inc.Drug Facts
Product Profile
Brand Name
mexiletine hydrochloride
Generic Name
mexiletine hydrochloride
Labeler
golden state medical supply, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
mexiletine hydrochloride 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51407-381
Product ID
51407-381_45b6d529-143e-2322-e063-6294a90a65a5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074450
Listing Expiration
2026-12-31
Marketing Start
1996-05-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51407381
Hyphenated Format
51407-381
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
mexiletine hydrochloride (source: ndc)
Generic Name
mexiletine hydrochloride (source: ndc)
Application Number
ANDA074450 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (51407-381-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45b6d529-143e-2322-e063-6294a90a65a5", "openfda": {"unii": ["606D60IS38"], "rxcui": ["1362706", "1362712", "1362720"], "spl_set_id": ["bfe2b847-e18d-cef2-e053-2995a90a42af"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (51407-381-01)", "package_ndc": "51407-381-01", "marketing_start_date": "20201218"}], "brand_name": "Mexiletine Hydrochloride", "product_id": "51407-381_45b6d529-143e-2322-e063-6294a90a65a5", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "51407-381", "generic_name": "Mexiletine Hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mexiletine Hydrochloride", "active_ingredients": [{"name": "MEXILETINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA074450", "marketing_category": "ANDA", "marketing_start_date": "19960516", "listing_expiration_date": "20261231"}