NDC 16729-372 – Tadalafil
Tadalafil 20 mg/1 · Tablet, Film Coated · Oral
Product NDC16729-372
Product details
- Brand name
- Tadalafil
- Generic name
- Tadalafil
- Labeler
- Accord Healthcare Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209167
- Marketed since
- March 27, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Phosphodiesterase 5 Inhibitor
Active ingredients
- Tadalafil 20 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 16729-372-10 | 30 TABLET, FILM COATED in 1 BOTTLE (16729-372-10) | Mar 27, 2019 |
| 16729-372-16 | 500 TABLET, FILM COATED in 1 BOTTLE (16729-372-16) | Apr 29, 2020 |
Recalls mentioning this NDC
- D-0416-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0414-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0417-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0415-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection.
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