Prescription drug · ANDA
Montelukast Sodium NDC 63187-430
Montelukast sodium 10 mg/1 · Tablet · Oral · Proficient Rx LP
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63187-430-30 | 6318704303063187043030 | 30 TABLET in 1 BOTTLE (63187-430-30)Marketed from Mar 3, 2014 | |
| 63187-430-60 | 6318704306063187043060 | 60 TABLET in 1 BOTTLE (63187-430-60)Marketed from Mar 3, 2014 | |
| 63187-430-90 | 6318704309063187043090 | 90 TABLET in 1 BOTTLE (63187-430-90)Marketed from Mar 3, 2014 |
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
- Route
- Oral
- Labeler
- Proficient Rx LPNDC labeler code 63187
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 201515
- Marketing start
- Listing expires
- Other FDA classes
- Leukotriene Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 63187-430_3987b125-2cd5-4cae-9009-4e839599a38eSPL ID 3987b125-2cd5-4cae-9009-4e839599a38eSPL set ID 8a724790-e1fb-4935-bb28-ce99455be5efRxCUI 200224UNII 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
N463187043030followed by a unit qualifier and the quantityPackage 63187-0430-30. 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 .
Indications (excerpt from the label)
1. INDICATIONS AND USAGE Montelukast sodium tablets are a leukotriene receptor antagonist indicated for: • Prophylaxisand chronic treatment of asthma inpatients 12 months of age and older(1.1 ). • Acuteprevention of exercise-induced bronchoconstriction(EIB) in patients 15 years of ageand older (1.2). • Relief'of symptoms of allergic rhinitis (AR):seasonal allergic rhinitis (SAR) in patients2 years of age and older , andperennial allergic rhinitis (PAR) in patients6 months of age and older (1.3). 1.1 Asthma Montelukast sodium is indicated for the prophylaxis and chronic treatment of asthma in adults and pediatric patients 12 months of age and older. 1.2 Exercise-Induced Bronchoconstriction Mo…
Excerpt only. Read the full label for complete information.
About NDC 63187-430
- What is NDC 63187-430?
- 63187-430 is the product NDC for Montelukast Sodium, Montelukast sodium 10 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 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?
- Proficient Rx LP, NDC labeler code 63187. 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 201515
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 | TabletOral | Torrent Pharmaceuticals Limited | 13668-081 |
| Montelukast Sodium | Montelukast sodium 10 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-8610 |