Sildenafil
- Product NDC
- 43063-668
- 11-digit product format
- 430630668
- Labeler code
- 43063
- Product ID
- 43063-668_efe40056-0386-6ce1-e053-2a95a90ab2e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA078380
- Marketing category
- ANDA
- Marketing start
- 2013-05-31
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43063-668 | SILDENAFIL TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.] | 19 | Legacy NDC | 20240606_30886aaa-4834-4a06-e054-00144ff8d46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-668-30 | 43063066830 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-668-30) | 2016-04-15 | 0000-00-00 | No | No | Current |