NDC 0078-0686 – Promacta
Eltrombopag Olamine 50 mg/1 · Tablet, Film Coated · Oral
Product NDC0078-0686
Product details
- Brand name
- Promacta
- Generic name
- Eltrombopag olamine
- Labeler
- Novartis Pharmaceuticals Corporation
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- NDA · NDA022291
- Marketed since
- April 7, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Thrombopoietin Receptor Agonist
Active ingredients
- Eltrombopag Olamine 50 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0078-0686-15 | 30 TABLET, FILM COATED in 1 BOTTLE (0078-0686-15) | Apr 7, 2016 |
| 0078-0686-55 | 14 TABLET, FILM COATED in 1 BOTTLE (0078-0686-55) | Jan 21, 2020 |
Recalls mentioning this NDC
- D-1309-2019 May 29, 2019 · Class I
Cross Contamination with Other Products: product is being recalled due to possible cross-contamination with peanut flour.
Other Promacta products
- 0078-0684 Eltrombopag Olamine 12.5 mg/1 · Tablet, Film Coated · Novartis Pharmaceuticals Corporation
- 0078-0685 Eltrombopag Olamine 25 mg/1 · Tablet, Film Coated · Novartis Pharmaceuticals Corporation
- 0078-0687 Eltrombopag Olamine 75 mg/1 · Tablet, Film Coated · Novartis Pharmaceuticals Corporation
- 0078-0697 Eltrombopag Olamine 25 mg/1 · Powder, For Suspension · Novartis Pharmaceuticals Corporation
- 0078-0972 Eltrombopag Olamine 12.5 mg/1 · Powder, For Suspension · Novartis Pharmaceuticals Corporation