Nilutamide
- Product NDC
- 82454-0212
- 11-digit product format
- 824540212
- Labeler code
- 82454
- Product ID
- 82454-0212_d326d8be-7f89-7a27-e053-2a95a90a5917
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nilutamide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CENEXI HSC
- Application
- NDA020169
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-11-22
- 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 |
|---|
| 82454-0212-3 | 82454021203 | 3 BLISTER PACK in 1 CARTON (82454-0212-3) > 10 TABLET in 1 BLISTER PACK | 3 blister pack | 2019-11-22 | 0000-00-00 | No | No | Current |