Montelukast sodium chewable is a Oral Tablet, Chewable in the Human Prescription Drug category. It is labeled and distributed by Jubilant Cadista Pharmaceuticals Inc.. The primary component is Montelukast Sodium.
Product ID | 59746-359_758593f9-d960-4ac8-8ada-02aeae115244 |
NDC | 59746-359 |
Product Type | Human Prescription Drug |
Proprietary Name | Montelukast sodium chewable |
Generic Name | Montelukast Sodium |
Dosage Form | Tablet, Chewable |
Route of Administration | ORAL |
Marketing Start Date | 2015-02-28 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA203795 |
Labeler Name | Jubilant Cadista Pharmaceuticals Inc. |
Substance Name | MONTELUKAST SODIUM |
Active Ingredient Strength | 5 mg/1 |
Pharm Classes | Leukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2015-02-28 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA203795 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-02-28 |
Marketing End Date | 2019-03-31 |
Marketing Category | ANDA |
Application Number | ANDA203795 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-02-28 |
Marketing End Date | 2019-03-31 |
Marketing Category | ANDA |
Application Number | ANDA203795 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-02-28 |
Marketing End Date | 2019-03-31 |
Marketing Category | ANDA |
Application Number | ANDA203795 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-02-28 |
Marketing End Date | 2019-03-31 |
Marketing Category | ANDA |
Application Number | ANDA203795 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-02-28 |
Marketing End Date | 2019-03-31 |
Marketing Category | ANDA |
Application Number | ANDA203795 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-02-28 |
Marketing End Date | 2019-03-31 |
Marketing Category | ANDA |
Application Number | ANDA203795 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-02-28 |
Marketing End Date | 2019-03-31 |
Ingredient | Strength |
---|---|
MONTELUKAST SODIUM | 5 mg/1 |
SPL SET ID: | 76d4a034-0082-1d94-5f92-6b071da7cadd |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
59746-358 | Montelukast sodium chewable | Montelukast sodium chewable |
59746-359 | Montelukast sodium chewable | Montelukast sodium chewable |
0054-0259 | Montelukast Sodium | Montelukast Sodium |
0054-0288 | Montelukast Sodium | Montelukast Sodium |
0054-0289 | Montelukast Sodium | Montelukast Sodium |
0093-7424 | Montelukast Sodium | Montelukast Sodium |
0093-7425 | Montelukast Sodium | Montelukast Sodium |
0006-1711 | SINGULAIR | montelukast sodium |
0006-3841 | SINGULAIR | montelukast sodium |
0006-9117 | SINGULAIR | montelukast sodium |
0006-9275 | SINGULAIR | montelukast sodium |