Zafirlukast
- Product NDC
- 0904-6646
- 11-digit product format
- 009046646
- Labeler code
- 0904
- Product ID
- 0904-6646_6cb5a2f5-4576-4eb7-bd77-0cd7854df76a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- zafirlukast
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- NDA020547
- Marketing category
- NDA
- Marketing start
- 2010-11-19
- Marketing end
- 0000-00-00
- Substance
- ZAFIRLUKAST
- Active strength
- 20 mg/1
- Pharmacologic classes
- Leukotriene Receptor Antagonists [MoA],Cytochrome P450 2C9 Inhibitors [MoA],Leukotriene Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6646-04 | 00904664604 | 30 BLISTER PACK in 1 CARTON (0904-6646-04) > 1 TABLET, COATED in 1 BLISTER PACK | 30 blister pack | 2010-11-19 | 0000-00-00 | No | No | Current |