NDC 16714-076 – Tadalafil
Tadalafil 10 mg/1 · Tablet, Film Coated · Oral
Product NDC16714-076
Product details
- Brand name
- Tadalafil
- Generic name
- Tadalafil
- Labeler
- NorthStar RxLLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208934
- Marketed since
- February 19, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Phosphodiesterase 5 Inhibitor
Active ingredients
- Tadalafil 10 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 16714-076-01 | 30 TABLET, FILM COATED in 1 BOTTLE (16714-076-01) | Feb 19, 2020 |
Recalls mentioning this NDC
- D-0231-2022 Nov 17, 2021 · Class II
Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product. - D-0230-2022 Nov 17, 2021 · Class II
Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.
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