Sildenafil Citrate
- Product NDC
- 50436-3500
- 11-digit product format
- 504363500
- Labeler code
- 50436
- Product ID
- 50436-3500_09e9dc1f-ec21-4f46-b322-9ae222aee44b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sildenafil citrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- NDA020895
- Marketing category
- NDA
- Marketing start
- 2017-12-01
- Marketing end
- 0000-00-00
- Substance
- SILDENAFIL CITRATE
- Active strength
- 50 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 |
|---|
| 50436-3500-1 | Sildenafil Citrate | 1080 in 1 CASE | TABLET, FILM COATED | 1080 | | 2 |
| 50436-3500-1 | Sildenafil Citrate | 1 in 1 POUCH | TABLET, FILM COATED | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-3500 | SILDENAFIL CITRATE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | Legacy NDC, 2 package rows | 20191120_7a4c81f9-826b-4d36-adc9-e6d8a839845e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-3500-1 | 50436350001 | 1080 in 1 CASE | Historical |