Sildenafil
- Product NDC
- 60687-416
- 11-digit product format
- 606870416
- Labeler code
- 60687
- Product ID
- 60687-416_ea3d0f00-3cf6-f047-e053-2995a90a33e6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA203814
- Marketing category
- ANDA
- Marketing start
- 2019-02-19
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60687-416-11 | Sildenafil | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 7 |
| 60687-416-21 | Sildenafil | 30 in 1 BOX, UNIT-DOSE | TABLET, FILM COATED | 30 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60687-416 | SILDENAFIL TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 6 | Legacy NDC, 2 package rows | 20241219_f7fbfc3b-807e-4375-a6eb-8db0eaf40c9c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-416-11 | 60687041611 | 1 in 1 BLISTER PACK | | | | | | Historical |
| 60687-416-21 | 60687041621 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-416-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-416-11) | 30 blister pack | 2019-02-19 | 0000-00-00 | No | No | Current |