Prescription drug · ANDA
Montelukast Sodium NDC 57237-255
Montelukast sodium 10 mg/1 · Tablet, Film coated · Oral · Rising Pharma Holdings, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 57237-255-30 | 5723702553057237025530 | 30 TABLET, FILM COATED in 1 BOTTLE (57237-255-30)Marketed from Aug 3, 2012 | |
| 57237-255-90 | 5723702559057237025590 | 90 TABLET, FILM COATED in 1 BOTTLE (57237-255-90)Marketed from Aug 3, 2012 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Montelukast Sodium
- Generic name (nonproprietary)
- montelukast sodium
- Active ingredients
- Montelukast sodium — 10 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Rising Pharma Holdings, Inc.NDC labeler code 57237
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 202468
- Marketing start
- Listing expires
- Other FDA classes
- Leukotriene Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 57237-255_b17c2611-11a0-4762-a99d-3552a93b79cdSPL ID b17c2611-11a0-4762-a99d-3552a93b79cdSPL set ID 49669ac0-0bb5-4576-bed5-9e85e0d76a44RxCUI 200224, 242438, 311759UNII U1O3J18SFL
- Pharmacologic class
- Leukotriene Receptor Antagonist
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N457237025530followed by a unit qualifier and the quantityPackage 57237-0255-30. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective . This label includes a boxed warning.
Indications (excerpt from the label)
Montelukast sodium is a leukotriene receptor antagonist indicated for: Prophylaxis and chronic treatment of asthma in patients 2 years of age and older ( 1.1 ). Acute prevention of exercise-induced bronchoconstriction (EIB) in patients 6 years of age and older ( 1.2 ). Relief of symptoms of allergic rhinitis (AR): seasonal allergic rhinitis (SAR) in patients 2 years of age and older, and perennial allergic rhinitis (PAR) in patients 2 years of age and older. Reserve use for patients who have an inadequate response or intolerance to alternative therapies ( 1.3 ). Limitations of Use: Not indicated to treat an acute asthma attack ( 5.2 ). 1.1 Asthma Montelukast sodium is indicated for the proph…
Excerpt only. Read the full label for complete information.
About NDC 57237-255
- What is NDC 57237-255?
- 57237-255 is the product NDC for Montelukast Sodium, Montelukast sodium 10 mg/1 tablet, film coated, listed with the FDA by Rising Pharma Holdings, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Montelukast Sodium.
- What is the active ingredient?
- Montelukast sodium.
- Who is the labeler?
- Rising Pharma Holdings, Inc., NDC labeler code 57237. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Montelukast Sodium?
- 70 other product NDCs are listed under this name. See all Montelukast Sodium NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Montelukast Sodium products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Montelukast Sodium | Montelukast sodium 10 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4753 | 70518-4753-00 |
| montelukast sodium | Montelukast sodium 10 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-8617 | 68788-8617-0368788-8617-0668788-8617-09 |
| Montelukast Sodium | Montelukast sodium 10 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-8610 | 68788-8610-0368788-8610-0668788-8610-09 |
| Montelukast Sodium | Montelukast sodium 10 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 16571-100 | 16571-0100-0916571-0100-10 |
| Montelukast Sodium | Montelukast sodium 10 mg/1 | Tablet, Film coatedOral | Direct_Rx | 72189-418 | 72189-0418-3072189-0418-90 |
| Montelukast Sodium | Montelukast 5 mg/1 | Tablet, ChewableOral | DIRECT RX | 72189-223 | 72189-0223-30 |
| Montelukast Sodiummontelukast | Montelukast sodium 4 mg/1 | Tablet, ChewableOral | Amneal Pharmaceuticals LLC | 65162-771 | 65162-0771-03 |
| Montelukast Sodiummontelukast | Montelukast sodium 5 mg/1 | Tablet, ChewableOral | Amneal Pharmaceuticals LLC | 65162-772 | 65162-0772-03 |
| montelukast sodium | Montelukast 5 mg/1 | Tablet, ChewableOral | Preferred Pharmaceuticals, Inc. | 68788-7669 | 68788-7669-0168788-7669-0268788-7669-03+3 more |
| Montelukast Sodium | Montelukast sodium 4 mg/1 | GranuleOral | Aurobindo Pharma Limited | 59651-329 | 59651-0329-30 |
Other NDCs under ANDA 202468
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Montelukast Sodium | Montelukast sodium 10 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 71205-778 |
| Montelukast Sodium | Montelukast sodium 10 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 72789-306 |