mefloquine hydrochloride

Generic: mefloquine hydrochloride

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mefloquine hydrochloride
Generic Name mefloquine hydrochloride
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

mefloquine hydrochloride 250 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0555-0171
Product ID 0555-0171_4b2b45f8-ed63-4b3c-87c5-801996f5b154
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076392
Listing Expiration 2027-12-31
Marketing Start 2004-01-06

Pharmacologic Class

Classes
antimalarial [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05550171
Hyphenated Format 0555-0171

Supplemental Identifiers

RxCUI
835913
UNII
5Y9L3636O3

Packaging Origin

Original Packager
true

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
  • 25 BLISTER PACK in 1 CARTON (0555-0171-78) / 1 TABLET in 1 BLISTER PACK (0555-0171-88)
source: ndc

Packages (1)

0555-0171-78 25 BLISTER PACK in 1 CARTON (0555-0171-78) / 1 TABLET in 1 BLISTER PACK (0555-0171-88)

Ingredients (1)

mefloquine hydrochloride (250 mg/1)

Linked Drug Pages (1)

Mefloquine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4b2b45f8-ed63-4b3c-87c5-801996f5b154", "openfda": {"unii": ["5Y9L3636O3"], "rxcui": ["835913"], "spl_set_id": ["09716a24-d7da-42b2-af29-c03a1b6670bd"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 BLISTER PACK in 1 CARTON (0555-0171-78)  / 1 TABLET in 1 BLISTER PACK (0555-0171-88)", "package_ndc": "0555-0171-78", "marketing_start_date": "20040106"}], "brand_name": "Mefloquine Hydrochloride", "product_id": "0555-0171_4b2b45f8-ed63-4b3c-87c5-801996f5b154", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]"], "product_ndc": "0555-0171", "generic_name": "Mefloquine Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "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": "20271231"}