Zafirlukast
- Product NDC
- 63629-2102
- 11-digit product format
- 636292102
- Labeler code
- 63629
- Product ID
- 63629-2102_2230ea91-0b0a-4b9a-a90d-a7e701e5814a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- zafirlukast
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA020547
- Marketing category
- NDA
- Marketing start
- 2010-11-19
- Marketing end
- 0000-00-00
- Substance
- ZAFIRLUKAST
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cytochrome P450 2C9 Inhibitors [MoA], Leukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2102-1 | 63629210201 | 60 TABLET, COATED in 1 BOTTLE (63629-2102-1) | 2021-01-29 | 0000-00-00 | No | No | Current |