Silodosin
- Product NDC
- 0781-2623
- 11-digit product format
- 007812623
- Labeler code
- 0781
- Product ID
- 0781-2623_1f5cc90a-3ca3-4e42-9210-cbb772746bfe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Silodosin
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA204726
- Marketing category
- ANDA
- Marketing start
- 2018-11-18
- Marketing end
- 0000-00-00
- Substance
- SILODOSIN
- Active strength
- 4 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-2623-10 | 00781262310 | 1000 CAPSULE, GELATIN COATED in 1 BOTTLE (0781-2623-10) | 2018-11-18 | 0000-00-00 | No | No | Current |
| 0781-2623-31 | 00781262331 | 30 CAPSULE, GELATIN COATED in 1 BOTTLE (0781-2623-31) | 2018-11-18 | 0000-00-00 | No | No | Current |
| 0781-2623-92 | 00781262392 | 90 CAPSULE, GELATIN COATED in 1 BOTTLE (0781-2623-92) | 2018-11-18 | 0000-00-00 | No | No | Current |