Silodosin
- Product NDC
- 71335-3128
- 11-digit product format
- 713353128
- Labeler code
- 71335
- Product ID
- 71335-3128_3163ca4a-fb52-422d-8678-d6e3e6e7ed7f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Silodosin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211166
- Marketing category
- ANDA
- Marketing start
- 2018-12-03
- Substance
- SILODOSIN
- Active strength
- 8 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Silodosin
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SILODOSIN | 8 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | CUZ39LUY82 |
| Rxcui | 809477 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-3128-1 | Silodosin | 30 in 1 BOTTLE | CAPSULE | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-3128-1 | 71335312801 | 30 CAPSULE in 1 BOTTLE (71335-3128-1) | 30 capsule | 2026-04-29 | No | No | Historical |