Sildenafil
- Product NDC
- 17224-460
- 11-digit product format
- 172240460
- Labeler code
- 17224
- Product ID
- 17224-460_89038c76-89bf-4667-b594-a3c9c82d2d71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- CALVIN, SCOTT AND COMPANY, INCORPORATED
- Application
- ANDA203814
- Marketing category
- ANDA
- Marketing start
- 2018-02-02
- Marketing end
- 0000-00-00
- Substance
- SILDENAFIL CITRATE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17224-460-28 | Sildenafil | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17224-460 | SILDENAFIL TABLET, FILM COATED [CALVIN, SCOTT AND COMPANY, INCORPORATED] | 1 | Legacy NDC, 1 package rows | 20191204_74ee9b44-aa9d-43af-88f7-da7e31ea0005.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 17224-460-28 | 17224046028 | 90 in 1 BOTTLE | Historical |