Nilutamide
- Product NDC
- 66993-212
- 11-digit product format
- 669930212
- Labeler code
- 66993
- Product ID
- 66993-212_c9e38096-18a3-4884-b918-a6b4b438f51e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nilutamide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Prasco Laboratories
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66993-212 | NILUTAMIDE TABLET [PRASCO LABORATORIES] | 3 | Legacy NDC | 20211218_34ea4810-2d6c-4bd9-ae52-8bab786dee91.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66993-212-38 | 66993021238 | 3 BLISTER PACK in 1 CARTON (66993-212-38) > 10 TABLET in 1 BLISTER PACK | 3 blister pack | 2019-11-22 | 0000-00-00 | No | No | Current |