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NDC 70518-2603-01 Montelukast 10 mg/1 Details
Montelukast 10 mg/1
Montelukast is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is MONTELUKAST SODIUM.
MedlinePlus Drug Summary
Montelukast is used to prevent wheezing, difficulty breathing, chest tightness, and coughing caused by asthma in adults and children 12 months of age and older. Montelukast is also used to prevent bronchospasm (breathing difficulties) during exercise in adults and children 6 years of age and older. Montelukast is also used to treat the symptoms of seasonal (occurs only at certain times of the year), allergic rhinitis (a condition associated with sneezing and stuffy, runny or itchy nose) in adults and children 2 years of age and older, and perennial (occurs all year round) allergic rhinitis in adults and children 6 months of age and older. Montelukast should be used to treat seasonal or perennial allergic rhinitis only in adults and children who cannot be treated with other medications. Montelukast is in a class of medications called leukotriene receptor antagonists (LTRAs). It works by blocking the action of substances in the body that cause the symptoms of asthma and allergic rhinitis.
Related Packages: 70518-2603-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Montelukast
Product Information
| NDC | 70518-2603 |
|---|---|
| Product ID | 70518-2603_048b0096-3e2f-12fd-e063-6394a90aefe8 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Montelukast |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Montelukast |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/1 |
| Substance Name | MONTELUKAST SODIUM |
| Labeler Name | REMEDYREPACK INC. |
| Pharmaceutical Class | Leukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA203366 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70518-2603-01 (70518260301)
| NDC Package Code | 70518-2603-1 |
|---|---|
| Billing NDC | 70518260301 |
| Package | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2603-1) |
| Marketing Start Date | 2020-03-27 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |