NDC 60290-030 – Tadalafil
Tadalafil 20 mg/1 · Tablet, Film Coated · Oral
Product NDC60290-030
Product details
- Brand name
- Tadalafil
- Generic name
- Tadalafil
- Labeler
- Umedica Laboratories USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211298
- Marketed since
- February 15, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Phosphodiesterase 5 Inhibitor
Active ingredients
- Tadalafil 20 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 60290-030-01 | 30 TABLET, FILM COATED in 1 BOTTLE (60290-030-01) | Feb 15, 2026 |
| 60290-030-02 | 1000 TABLET, FILM COATED in 1 BOTTLE (60290-030-02) | Feb 15, 2026 |
| 60290-030-03 | 30 TABLET, FILM COATED in 1 BLISTER PACK (60290-030-03) | Feb 15, 2026 |
| 60290-030-04 | 500 TABLET, FILM COATED in 1 BOTTLE (60290-030-04) | Apr 24, 2026 |
| 60290-030-05 | 5000 TABLET, FILM COATED in 1 BOTTLE (60290-030-05) | Apr 24, 2026 |
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