Montelukast Sodium
- Product NDC
- 55154-4380
- 11-digit product format
- 551544380
- Labeler code
- 55154
- Product ID
- 55154-4380_79928dc8-f03d-48cd-9d70-c6acd7810a45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- montelukast sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA079103
- Marketing category
- ANDA
- Marketing start
- 2012-08-29
- 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
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record