eltrombopag

Generic: eltrombopag olamine

Labeler: novadoz pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name eltrombopag
Generic Name eltrombopag olamine
Labeler novadoz pharmaceuticals llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

eltrombopag olamine 75 mg/1

Manufacturer
Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-159
Product ID 72205-159_5a9ec8c8-3c0b-4f11-848c-c04ccee0d44f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA220250
Listing Expiration 2027-12-31
Marketing Start 2026-01-14

Pharmacologic Class

Classes
breast cancer resistance protein inhibitors [moa] increased megakaryocyte maturation [pe] increased platelet production [pe] organic anion transporting polypeptide 1b1 inhibitors [moa] thrombopoietin receptor agonist [epc] thrombopoietin receptor agonists [moa] ugt1a1 inhibitors [moa] ugt1a3 inhibitors [moa] ugt1a4 inhibitors [moa] ugt1a6 inhibitors [moa] ugt1a9 inhibitors [moa] ugt2b15 inhibitors [moa] ugt2b7 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72205159
Hyphenated Format 72205-159

Supplemental Identifiers

RxCUI
825421 825427 884617 1245001
UPC
0372205159303 0372205158191 0372205157309 0372205158306
UNII
4U07F515LG

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name eltrombopag (source: ndc)
Generic Name eltrombopag olamine (source: ndc)
Application Number ANDA220250 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (72205-159-30)
source: ndc

Packages (1)

72205-159-30 30 TABLET, FILM COATED in 1 BOTTLE (72205-159-30)

Ingredients (1)

eltrombopag olamine (75 mg/1)

Linked Drug Pages (1)

eltrombopag ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5a9ec8c8-3c0b-4f11-848c-c04ccee0d44f", "openfda": {"upc": ["0372205159303", "0372205158191", "0372205157309", "0372205158306"], "unii": ["4U07F515LG"], "rxcui": ["825421", "825427", "884617", "1245001"], "spl_set_id": ["5a9ec8c8-3c0b-4f11-848c-c04ccee0d44f"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72205-159-30)", "package_ndc": "72205-159-30", "marketing_start_date": "20260114"}], "brand_name": "eltrombopag", "product_id": "72205-159_5a9ec8c8-3c0b-4f11-848c-c04ccee0d44f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Breast Cancer Resistance Protein Inhibitors [MoA]", "Increased Megakaryocyte Maturation [PE]", "Increased Platelet Production [PE]", "Organic Anion Transporting Polypeptide 1B1 Inhibitors [MoA]", "Thrombopoietin Receptor Agonist [EPC]", "Thrombopoietin Receptor Agonists [MoA]", "UGT1A1 Inhibitors [MoA]", "UGT1A3 Inhibitors [MoA]", "UGT1A4 Inhibitors [MoA]", "UGT1A6 Inhibitors [MoA]", "UGT1A9 Inhibitors [MoA]", "UGT2B15 Inhibitors [MoA]", "UGT2B7 Inhibitors [MoA]"], "product_ndc": "72205-159", "generic_name": "eltrombopag olamine", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "eltrombopag", "active_ingredients": [{"name": "ELTROMBOPAG OLAMINE", "strength": "75 mg/1"}], "application_number": "ANDA220250", "marketing_category": "ANDA", "marketing_start_date": "20260114", "listing_expiration_date": "20271231"}