NDC 55111-763-07 - Montelukast Sodium

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
55111-763
Requested NDC
55111-763-07
Package NDCs from labels
55111-763-07, 55111-763-03
Manufacturer
Dr.Reddy's Laboratories Limited | Dr.Reddy's Laboratories Limited-FTO3
Effective date
2019-08-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Montelukast Sodium - Dr.Reddy's Laboratories Limited | Dr.Reddy's Laboratories Limited-FTO3Dr.Reddy's Laboratories Limited | Dr.Reddy's Laboratories Limited-FTO32019-08-30HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unitNational Council for Prescription Drug Programs2013-02-13Indexing - Billing Unit

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55111-763-03Montelukast Sodium30 in 1 CARTONGRANULE3015
55111-763-07Montelukast Sodium500 in 1 PACKETGRANULE50015

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55111-763MONTELUKAST SODIUM GRANULE [DR.REDDY'S LABORATORIES LIMITED]15Legacy NDC, 2 package rows20190920_3d3df874-d710-7fa4-bb21-434977518337.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55111-763-03EA - Each55111-763569ceb14-5889-4aeb-804d-5c1cac519e0412013-02-13
55111-763-07EA - Each55111-763ef749b31-25f5-4d9c-a7e2-3dadf931d5bf12013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Montelukast SodiumACTIVE INGREDIENTU1O3J18SFLMONTELUKAST SODIUM GRANULE [DR.REDDY'S LABORATORIES LIMITED]12
montelukastACTIVE MOIETYMHM278SD3EMONTELUKAST SODIUM GRANULE [DR.REDDY'S LABORATORIES LIMITED]12
HYPROMELLOSE 2910 (3 MPA.S)INACTIVE INGREDIENT0VUT3PMY82MONTELUKAST SODIUM GRANULE [DR.REDDY'S LABORATORIES LIMITED]12
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30MONTELUKAST SODIUM GRANULE [DR.REDDY'S LABORATORIES LIMITED]12
MANNITOLINACTIVE INGREDIENT3OWL53L36AMONTELUKAST SODIUM GRANULE [DR.REDDY'S LABORATORIES LIMITED]12

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 4 · 68 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MontelukastMONTELUKASTCoupler LLC583a9499-97f0-2ebf-e063-6394a90a35af2026-08-04Boxed warning, Warnings, Adverse reactionsExact identifier
unii: U1O3J18SFL
Montelukast SodiumMONTELUKAST SODIUMTorrent Pharmaceuticals Limitedda038cf6-cfad-43a4-ab8e-d81d028d60872026-07-28Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 351246
unii: U1O3J18SFL
montelukast sodiumMONTELUKAST SODIUMPreferred Pharmaceuticals Inc.1eeb3123-9e93-4681-8096-800a7c7acf8a2026-07-28Boxed warning, Warnings, Adverse reactionsExact identifier
unii: U1O3J18SFL
MontelukastMONTELUKASTPreferred Pharmaceuticals, Inc.94642db1-5c75-44c4-92b4-8385b486df822026-07-28Boxed warning, Warnings, Adverse reactionsExact identifier
unii: U1O3J18SFL
Montelukast SodiumMONTELUKAST SODIUMPreferred Pharmaceuticals Inc.64a3b181-e8d8-4caf-9f1b-e0063d0bd94a2026-07-28Boxed warning, Warnings, Adverse reactionsExact identifier
unii: U1O3J18SFL
Montelukast SodiumMONTELUKAST SODIUMRising Pharma Holdings, Inc.49669ac0-0bb5-4576-bed5-9e85e0d76a442026-05-29Boxed warning, Warnings, Adverse reactionsExact identifier
unii: U1O3J18SFL
MannitolMANNITOLHospira, Inc.8ad3145e-00e7-4412-b9a5-06f00f264f302026-04-21Warnings, Adverse reactionsExact identifier
unii: 3OWL53L36A
MontelukastMONTELUKASTREMEDYREPACK INC.ecaa9b4b-5941-4af5-930c-35e9f3b2b4ba2026-04-03Boxed warning, Warnings, Adverse reactionsExact identifier
unii: U1O3J18SFL
MontelukastMONTELUKASTAvPAKd7870c45-5a8b-8369-e053-2a95a90ae1f32026-01-08Boxed warning, Warnings, Adverse reactionsExact identifier
unii: U1O3J18SFL
Montelukast SodiumMONTELUKAST SODIUMRedpharm Drug2fbdf1be-a37f-879b-e063-6394a90aa20d2025-12-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: U1O3J18SFL
MONTELUKAST SODIUMMONTELUKAST SODIUMChartwell RX, LLC5cb4298c-10b1-4d6f-95ad-4aad72daf2492025-12-17Boxed warning, Warnings, Adverse reactionsExact identifier
unii: U1O3J18SFL
Montelukast SodiumMONTELUKAST SODIUMAvKAREed2caffa-a75c-1c27-ae30-2d8280eaea7d2025-12-16Warnings, Adverse reactionsExact identifier
unii: U1O3J18SFL
MONTELUKASTMONTELUKAST SODIUMA-S Medication Solutionsda9821f1-536a-416b-9594-210bde0cefaf2025-12-11Boxed warning, Warnings, Adverse reactionsExact identifier
unii: U1O3J18SFL
QR PAINANALGESICMARYHELENE ENTERPRISES INC8f8f53e3-fe31-e7b5-e053-2995a90a710d2025-11-14WarningsExact identifier
unii: 3OWL53L36A
QR PAINANALGESICMARYHELENE ENTERPRISES INC9984a510-30be-4013-e053-2995a90a841e2025-11-14WarningsExact identifier
unii: 3OWL53L36A
MannitolMANNITOLProPharma Distribution430669d7-9ad1-9a04-e063-6394a90ababb2025-11-07Warnings, Adverse reactionsExact identifier
unii: 3OWL53L36A
Sorbitol-MannitolSORBITOL AND MANNITOLICU Medical Inc.5b44e248-4b7b-4777-954a-921c7b3099442025-10-30Warnings, Adverse reactionsExact identifier
unii: 3OWL53L36A
Montelukast SodiumMONTELUKAST SODIUMAvPAK2f90a573-27fd-cc16-f3d1-8c4d630224a02025-10-29Warnings, Adverse reactionsExact identifier
unii: U1O3J18SFL
MannitolMANNITOLICU Medical Inc.ba7bf864-8a4d-4262-8fd1-00174fa2f9d12025-10-24Warnings, Adverse reactionsExact identifier
unii: 3OWL53L36A
Montelukast SodiumMONTELUKAST SODIUMPD-Rx Pharmaceuticals, Inc.c9ec1996-6a54-4622-b8a6-57dea49f6b352025-10-16Boxed warning, Warnings, Adverse reactionsExact identifier
unii: U1O3J18SFL

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.