mefloquine hydrochloride

Generic: mefloquine hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mefloquine hydrochloride
Generic Name mefloquine hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

mefloquine hydrochloride 250 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2396
Product ID 50090-2396_4c4467e1-5886-4b66-aaff-8647a8591fce
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076392
Listing Expiration 2026-12-31
Marketing Start 2004-01-06

Pharmacologic Class

Classes
antimalarial [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500902396
Hyphenated Format 50090-2396

Supplemental Identifiers

RxCUI
835913
UNII
5Y9L3636O3

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 mefloquine hydrochloride (source: ndc)
Generic Name mefloquine hydrochloride (source: ndc)
Application Number ANDA076392 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (50090-2396-0) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

mefloquine hydrochloride (250 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c4467e1-5886-4b66-aaff-8647a8591fce", "openfda": {"unii": ["5Y9L3636O3"], "rxcui": ["835913"], "spl_set_id": ["9cbe26c7-7313-4cd6-9514-9190af1de763"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-2396-0)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "50090-2396-0", "marketing_start_date": "20160506"}], "brand_name": "Mefloquine Hydrochloride", "product_id": "50090-2396_4c4467e1-5886-4b66-aaff-8647a8591fce", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]"], "product_ndc": "50090-2396", "generic_name": "Mefloquine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mefloquine Hydrochloride", "active_ingredients": [{"name": "MEFLOQUINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA076392", "marketing_category": "ANDA", "marketing_start_date": "20040106", "listing_expiration_date": "20261231"}