Nilandron
- Product NDC
- 82454-0111
- 11-digit product format
- 824540111
- Labeler code
- 82454
- Product ID
- 82454-0111_d44e4842-09c8-72e9-e053-2a95a90a7c44
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nilutamide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CENEXI HSC
- Application
- NDA020169
- Marketing category
- NDA
- Marketing start
- 2013-07-15
- Marketing end
- 0000-00-00
- Substance
- NILUTAMIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Androgen Receptor Antagonists [MoA],Androgen Receptor Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 82454-0111-1 | 82454011101 | 3 BLISTER PACK in 1 CARTON (82454-0111-1) > 10 TABLET in 1 BLISTER PACK | 3 blister pack | 2013-07-15 | 0000-00-00 | No | No | Current |