NDC 51655-473 – Tadalafil
Tadalafil 20 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-473
Product details
- Brand name
- Tadalafil
- Generic name
- Tadalafil
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209167
- Marketed since
- November 6, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Phosphodiesterase 5 Inhibitor
Active ingredients
- Tadalafil 20 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51655-473-54 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-473-54) | Nov 6, 2020 |
| 51655-473-87 | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-473-87) | Nov 6, 2020 |
Recalls mentioning this NDC
- D-0553-2023 May 3, 2023 · Class II
CGMP Deviations
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