NDC Product
Human Prescription DrugEltrombopag Olamine NDC 60219-1414
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Directory Crossover & Product Mapping
The following National Drug Codes (NDCs) are directly associated with the clinical concept for Eltrombopag 25 mg Oral Tablet (RxCUI 825421). This crossover tool provides a verified mapping between standardized RxNorm clinical drug definitions and the specific manufactured products listed in the FDA NDC directory.
Healthcare professionals, pharmacists, and data analysts use this list to identify various brand names, labelers, and commercial packaging variations linked to this semantic clinical drug concept. Each entry below represents a commercial product that fulfills the requirements of this specific clinical identifier.
Manufacturer Quick Index
Found 50 manufactured products
Amneal Pharmaceuticals NY LLC
Active Listing
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 60219-1415
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 60219-1416
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 60219-1417
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 69238-1414
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 69238-1415
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 69238-1416
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 69238-1417
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvKARE
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 42291-932
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 42291-933
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 42291-934
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 42291-935
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugEltrombopag NDC 31722-841
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 31722-842
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 31722-843
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 31722-844
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Dr. Reddy's Laboratories Inc.,
NDC Product
Human Prescription DrugEltrombopag NDC 43598-151
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 43598-730
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 43598-731
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 43598-732
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugEltrombopag NDC 0054-0962
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 0054-0963
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 0054-0964
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 0054-0965
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Novadoz Pharmaceuticals LLC
NDC Product
Human Prescription DrugEltrombopag NDC 72205-156
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 72205-157
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 72205-158
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 72205-159
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugPromacta NDC 0078-0684
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPromacta NDC 0078-0685
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPromacta NDC 0078-0686
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPromacta NDC 0078-0687
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPromacta NDC 0078-0697
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPromacta NDC 0078-0972
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
Somerset Therapeutics, LLC
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 70069-837
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 70069-838
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 70069-839
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag Olamine NDC 70069-840
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
XLCare Pharmaceuticals Inc.
NDC Product
Human Prescription DrugEltrombopag NDC 72865-299
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 72865-300
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 72865-301
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 72865-302
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Zydus Lifesciences Limited
NDC Product
Human Prescription DrugEltrombopag NDC 70771-1925
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 70771-1926
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 70771-1927
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 70771-1928
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Zydus Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugEltrombopag NDC 70710-1395
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 70710-1396
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 70710-1397
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 70710-1398
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
