mefloquine hydrochloride
Generic: mefloquine hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
mefloquine hydrochloride
Generic Name
mefloquine hydrochloride
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
mefloquine hydrochloride 250 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500902396
Hyphenated Format
50090-2396
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
mefloquine hydrochloride (source: ndc)
Generic Name
mefloquine hydrochloride (source: ndc)
Application Number
ANDA076392 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 1 BLISTER PACK in 1 CARTON (50090-2396-0) / 10 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (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"}