eltrombopag
Generic: eltrombopag olamine
Labeler: camber pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
eltrombopag
Generic Name
eltrombopag olamine
Labeler
camber pharmaceuticals, inc.
Dosage Form
POWDER, FOR SUSPENSION
Routes
Active Ingredients
eltrombopag olamine 12.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
31722-300
Product ID
31722-300_315730ec-c40c-af1a-e063-6294a90a010f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216620
Listing Expiration
2026-12-31
Marketing Start
2025-05-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
31722300
Hyphenated Format
31722-300
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA216620 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 12.5 mg/1
Packaging
- 1 CARTON in 1 KIT (31722-300-32) / 30 PACKET in 1 CARTON (31722-300-31) / 1 POWDER, FOR SUSPENSION in 1 PACKET (31722-300-12)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "315730ec-c40c-af1a-e063-6294a90a010f", "openfda": {"upc": ["0331722301251", "0331722300124"], "unii": ["4U07F515LG"], "rxcui": ["1859498", "2058980"], "spl_set_id": ["8f6499f0-4774-4f1e-8ab5-145c1fe64401"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 CARTON in 1 KIT (31722-300-32) / 30 PACKET in 1 CARTON (31722-300-31) / 1 POWDER, FOR SUSPENSION in 1 PACKET (31722-300-12)", "package_ndc": "31722-300-32", "marketing_start_date": "20250513"}], "brand_name": "Eltrombopag", "product_id": "31722-300_315730ec-c40c-af1a-e063-6294a90a010f", "dosage_form": "POWDER, FOR SUSPENSION", "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": "31722-300", "generic_name": "Eltrombopag olamine", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eltrombopag", "active_ingredients": [{"name": "ELTROMBOPAG OLAMINE", "strength": "12.5 mg/1"}], "application_number": "ANDA216620", "marketing_category": "ANDA", "marketing_start_date": "20250513", "listing_expiration_date": "20261231"}