Sildenafil
- Product NDC
- 63739-072
- 11-digit product format
- 637390072
- Labeler code
- 63739
- Product ID
- 63739-072_db62a327-1d6d-6bb2-e053-2995a90a4600
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA203623
- Marketing category
- ANDA
- Marketing start
- 2022-03-29
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63739-072 | SILDENAFIL TABLET, FILM COATED [MCKESSON CORPORATION DBA SKY PACKAGING] | 9 | Legacy NDC | 20250115_db62a327-1d96-6bb2-e053-2995a90a4600.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-072-33 | 63739007233 | 3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-072-33) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 3 blister pack | 2022-03-29 | 0000-00-00 | No | No | Current |