montelukast sodium

Generic: montelukast sodium

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name montelukast sodium
Generic Name montelukast sodium
Labeler rising pharma holdings, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

montelukast sodium 10 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 57237-255
Product ID 57237-255_1da56873-29ff-4b62-bebb-123a87d0e042
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202468
Listing Expiration 2026-12-31
Marketing Start 2012-08-03

Pharmacologic Class

Classes
leukotriene receptor antagonist [epc] leukotriene receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 57237255
Hyphenated Format 57237-255

Supplemental Identifiers

RxCUI
200224 242438 311759
UNII
U1O3J18SFL

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 montelukast sodium (source: ndc)
Generic Name montelukast sodium (source: ndc)
Application Number ANDA202468 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (57237-255-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (57237-255-90)
source: ndc

Packages (2)

57237-255-30 30 TABLET, FILM COATED in 1 BOTTLE (57237-255-30) 57237-255-90 90 TABLET, FILM COATED in 1 BOTTLE (57237-255-90)

Ingredients (1)

montelukast sodium (10 mg/1)

Linked Drug Pages (1)

Montelukast Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1da56873-29ff-4b62-bebb-123a87d0e042", "openfda": {"unii": ["U1O3J18SFL"], "rxcui": ["200224", "242438", "311759"], "spl_set_id": ["49669ac0-0bb5-4576-bed5-9e85e0d76a44"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (57237-255-30)", "package_ndc": "57237-255-30", "marketing_start_date": "20120803"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (57237-255-90)", "package_ndc": "57237-255-90", "marketing_start_date": "20120803"}], "brand_name": "Montelukast Sodium", "product_id": "57237-255_1da56873-29ff-4b62-bebb-123a87d0e042", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "57237-255", "generic_name": "Montelukast Sodium", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Montelukast Sodium", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA202468", "marketing_category": "ANDA", "marketing_start_date": "20120803", "listing_expiration_date": "20261231"}