NDC 68001-363 – Sildenafil
Sildenafil Citrate 20 mg/1 · Tablet, Film Coated · Oral
Product NDC68001-363
Product details
- Brand name
- Sildenafil
- Generic name
- Sildenafil
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203814
- Marketed since
- September 14, 2018
- Marketing end
- October 31, 2027
- Pharmacologic class
- Phosphodiesterase 5 Inhibitor
Active ingredients
- Sildenafil Citrate 20 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68001-363-05 | 90 TABLET, FILM COATED in 1 BOTTLE (68001-363-05) | Sep 14, 2018 |
Other Sildenafil products
- 50090-5235 Sildenafil Citrate 25 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-5236 Sildenafil Citrate 20 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-5325 Sildenafil Citrate 100 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-6804 Sildenafil Citrate 50 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-5415 Sildenafil Citrate 50 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7963 Sildenafil Citrate 25 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7964 Sildenafil Citrate 100 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-7977 Sildenafil Citrate 50 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 72888-015 Sildenafil Citrate 25 mg/1 · Tablet, Film Coated · Advagen Pharma Ltd
- 72888-017 Sildenafil Citrate 100 mg/1 · Tablet, Film Coated · Advagen Pharma Ltd
- 72888-016 Sildenafil Citrate 50 mg/1 · Tablet, Film Coated · Advagen Pharma Ltd
- 60687-788 Sildenafil Citrate 20 mg/1 · Tablet, Film Coated · American Health Packaging