mexiletine hydrochloride
Generic: mexiletine hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
mexiletine hydrochloride
Generic Name
mexiletine hydrochloride
Labeler
bryant ranch prepack
Dosage Form
CAPSULE
Routes
Active Ingredients
mexiletine hydrochloride 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-1773
Product ID
72162-1773_b32e1416-4347-47ea-a4ed-69983070e7ef
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074450
Listing Expiration
2026-12-31
Marketing Start
2020-06-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721621773
Hyphenated Format
72162-1773
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
- 200 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (72162-1773-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b32e1416-4347-47ea-a4ed-69983070e7ef", "openfda": {"unii": ["606D60IS38"], "rxcui": ["1362712"], "spl_set_id": ["a0bd3f2c-44e5-4ad0-9b76-c2028f0cae11"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-1773-1)", "package_ndc": "72162-1773-1", "marketing_start_date": "20240207"}], "brand_name": "Mexiletine Hydrochloride", "product_id": "72162-1773_b32e1416-4347-47ea-a4ed-69983070e7ef", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "72162-1773", "generic_name": "Mexiletine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mexiletine Hydrochloride", "active_ingredients": [{"name": "MEXILETINE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA074450", "marketing_category": "ANDA", "marketing_start_date": "20200622", "listing_expiration_date": "20261231"}