NDC 68180-914 – Tadalafil
Tadalafil 20 mg/1 · Tablet, Film Coated · Oral
Product NDC68180-914
Product details
- Brand name
- Tadalafil
- Generic name
- Tadalafil
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA210572
- Marketed since
- February 11, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Phosphodiesterase 5 Inhibitor
Active ingredients
- Tadalafil 20 mg/1
Package NDC codes (0)
| Package NDC | Description | Since |
|---|
Other Tadalafil products
- 50090-4660 Tadalafil 5 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7314 Tadalafil 5 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7390 Tadalafil 5 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7391 Tadalafil 5 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-8047 Tadalafil 20 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-8039 Tadalafil 20 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-6150 Tadalafil 20 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7315 Tadalafil 5 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-6945 Tadalafil 5 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 16729-371 Tadalafil 10 mg/1 · Tablet, Film Coated · Accord Healthcare Inc.
- 16729-369 Tadalafil 2.5 mg/1 · Tablet, Film Coated · Accord Healthcare Inc.
- 16729-370 Tadalafil 5 mg/1 · Tablet, Film Coated · Accord Healthcare Inc.