Details for New Drug Application (NDA): 208621
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The generic ingredient in MONTELUKAST SODIUM is montelukast sodium. There are thirty-five drug master file entries for this compound. Thirty-nine suppliers are listed for this compound. Additional details are available on the montelukast sodium profile page.
Summary for 208621
| Tradename: | MONTELUKAST SODIUM |
| Applicant: | Unichem |
| Ingredient: | montelukast sodium |
| Patents: | 0 |
Pharmacology for NDA: 208621
| Mechanism of Action | Leukotriene Receptor Antagonists |
Suppliers and Packaging for NDA: 208621
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| MONTELUKAST SODIUM | montelukast sodium | TABLET, CHEWABLE;ORAL | 208621 | ANDA | Unichem Pharmaceuticals (USA), Inc. | 29300-221 | 29300-221-10 | 1000 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (29300-221-10) |
| MONTELUKAST SODIUM | montelukast sodium | TABLET, CHEWABLE;ORAL | 208621 | ANDA | Unichem Pharmaceuticals (USA), Inc. | 29300-221 | 29300-221-13 | 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (29300-221-13) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, CHEWABLE;ORAL | Strength | EQ 4MG BASE | ||||
| Approval Date: | Jul 2, 2018 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, CHEWABLE;ORAL | Strength | EQ 5MG BASE | ||||
| Approval Date: | Jul 2, 2018 | TE: | AB | RLD: | No | ||||
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