montelukast sodium

Product NDC
68462-392
11-digit product format
684620392
Labeler code
68462
Product ID
68462-392_f0d0622b-cef1-4983-95df-09219e08530b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
montelukast sodium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Glenmark Pharmaceuticals Inc., USA
Application
ANDA090926
Marketing category
ANDA
Marketing start
2012-08-03
Marketing end
0000-00-00
Substance
MONTELUKAST SODIUM
Active strength
10 mg/1
Pharmacologic classes
Leukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
8d8a355b-240d-8c38-7331-c9e3c1068a33Product name920161220

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68462-392-05EA - Each68462-39247c48632-18b6-4545-aeb1-ca81643c820512013-02-13
68462-392-30EA - Each68462-392b0f550e0-9878-4a00-a2fc-a60295e93e7512013-02-13
68462-392-90EA - Each68462-392585c2913-2eb5-4db8-9cb6-f31d8b10c62712013-02-13

DailyMed Socrata Ingredients#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
200224montelukast sodium 10 MG Oral TabletPSNf3f3ee81-2530-402f-9c0a-c828fda2ca1f1
200224montelukast 10 MG Oral TabletSCDf3f3ee81-2530-402f-9c0a-c828fda2ca1f1
200224montelukast 10 MG (as montelukast sodium 10.4 MG) Oral TabletSYf3f3ee81-2530-402f-9c0a-c828fda2ca1f1