Montelukast Sodium
- Product NDC
- 68151-3498
- 11-digit product format
- 681513498
- Labeler code
- 68151
- Product ID
- 68151-3498_0d08efe6-84cb-459e-9591-0b85ddd8cd5f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Montelukast Sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA091576
- Marketing category
- ANDA
- Marketing start
- 2012-08-03
- Marketing end
- 0000-00-00
- Substance
- MONTELUKAST SODIUM
- Active strength
- 10 mg/1
- Pharmacologic classes
- Leukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68151-3498-2 | Montelukast Sodium | 1 in 1 CUP | TABLET, FILM COATED | 1 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-3498 | MONTELUKAST SODIUM TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT] | 7 | Legacy NDC, 1 package rows | 20160227_fe6bd2eb-3e27-4f55-988c-06d229334646.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-3498-2 | 68151349802 | 1 in 1 CUP | Historical |