Sildenafil
- Product NDC
- 70518-2128
- 11-digit product format
- 705182128
- Labeler code
- 70518
- Product ID
- 70518-2128_c624e283-b904-11f3-e053-2995a90ac629
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202659
- Marketing category
- ANDA
- Marketing start
- 2019-06-04
- Marketing end
- 0000-00-00
- Substance
- SILDENAFIL CITRATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2128 | SILDENAFIL TABLET, FILM COATED [REMEDYREPACK INC.] | 9 | Legacy NDC | 20250308_6a104328-3208-4157-be60-8fdc907d3825.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2128-0 | 70518212800 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2128-0) | 2019-06-04 | 0000-00-00 | No | No | Current |
| 70518-2128-1 | 70518212801 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2128-1) | 2019-06-04 | 0000-00-00 | No | No | Current |
| 70518-2128-2 | 70518212802 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2128-2) | 2019-06-14 | 0000-00-00 | No | No | Current |
| 70518-2128-3 | 70518212803 | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2128-3) | 2019-08-09 | 0000-00-00 | No | No | Current |