Flutamide
- Product NDC
- 49884-753
- 11-digit product format
- 498840753
- Labeler code
- 49884
- Product ID
- 49884-753_0d184d29-fbaf-4d17-98bc-13852fc67a9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flutamide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA075298
- Marketing category
- ANDA
- Marketing start
- 2006-01-26
- Marketing end
- 2023-08-31
- Substance
- FLUTAMIDE
- Active strength
- 125 mg/1
- Pharmacologic classes
- Androgen Receptor Antagonists [MoA], Androgen Receptor Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 49884-753-13 | 49884075313 | 180 CAPSULE in 1 BOTTLE (49884-753-13) | 180 capsule | 2006-01-26 | 2023-08-31 | No | No | Current |