mefloquine hydrochloride
Generic: mefloquine hydrochloride
Labeler: chartwell rx, llcDrug Facts
Product Profile
Brand Name
mefloquine hydrochloride
Generic Name
mefloquine hydrochloride
Labeler
chartwell rx, llc
Dosage Form
TABLET
Routes
Active Ingredients
mefloquine hydrochloride 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62135-973
Product ID
62135-973_2732839a-191a-570f-e063-6294a90a40a4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076175
Listing Expiration
2026-12-31
Marketing Start
2022-02-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62135973
Hyphenated Format
62135-973
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA076175 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 5 TABLET in 1 BOTTLE (62135-973-11)
- 25 TABLET in 1 BOTTLE (62135-973-25)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2732839a-191a-570f-e063-6294a90a40a4", "openfda": {"upc": ["0362135973117", "0362135973254"], "unii": ["5Y9L3636O3"], "rxcui": ["835913"], "spl_set_id": ["b884d22b-aae7-4f14-9a04-ae4029a229f0"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 TABLET in 1 BOTTLE (62135-973-11)", "package_ndc": "62135-973-11", "marketing_start_date": "20241115"}, {"sample": false, "description": "25 TABLET in 1 BOTTLE (62135-973-25)", "package_ndc": "62135-973-25", "marketing_start_date": "20241115"}], "brand_name": "Mefloquine Hydrochloride", "product_id": "62135-973_2732839a-191a-570f-e063-6294a90a40a4", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]"], "product_ndc": "62135-973", "generic_name": "Mefloquine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mefloquine Hydrochloride", "active_ingredients": [{"name": "MEFLOQUINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA076175", "marketing_category": "ANDA", "marketing_start_date": "20220220", "listing_expiration_date": "20261231"}