Eltrombopag

Product NDC
70377-183
11-digit product format
703770183
Labeler code
70377
Product ID
70377-183_d3dd9b3b-e4c2-90e7-f22a-53b70f494f65
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Eltrombopag
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Biocon Pharma Inc.
Application
ANDA220660
Marketing category
ANDA
Marketing start
2026-09-09
Substance
ELTROMBOPAG OLAMINE
Active strength
12.5 mg/1
Pharmacologic 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]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 4 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A220660-001ELTROMBOPAG OLAMINEELTROMBOPAG OLAMINEEQ 12.5MG ACIDTABLET / ORALAB2026-04-28
A220660-002ELTROMBOPAG OLAMINEELTROMBOPAG OLAMINEEQ 25MG ACIDTABLET / ORALAB2026-04-28
A220660-003ELTROMBOPAG OLAMINEELTROMBOPAG OLAMINEEQ 50MG ACIDTABLET / ORALAB2026-04-28
A220660-004ELTROMBOPAG OLAMINEELTROMBOPAG OLAMINEEQ 75MG ACIDTABLET / ORALAB2026-04-28

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 4 matching rows.

Application-product, TE code table
Application-productTE code
A220660-001AB
A220660-002AB
A220660-003AB
A220660-004AB

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A220660-001ELTROMBOPAG OLAMINEEQ 12.5MG ACIDTABLET / ORALAB2026-04-2884e616aacf4f…
2026-09-14 22:38:342026-08A220660-002ELTROMBOPAG OLAMINEEQ 25MG ACIDTABLET / ORALAB2026-04-2884e616aacf4f…
2026-09-14 22:38:342026-08A220660-003ELTROMBOPAG OLAMINEEQ 50MG ACIDTABLET / ORALAB2026-04-2884e616aacf4f…
2026-09-14 22:38:342026-08A220660-004ELTROMBOPAG OLAMINEEQ 75MG ACIDTABLET / ORALAB2026-04-2884e616aacf4f…
2026-08-18 06:07:402026-07A220660-001ELTROMBOPAG OLAMINEEQ 12.5MG ACIDTABLET / ORALAB2026-04-28caaa826d4ba7…
2026-08-18 06:07:402026-07A220660-002ELTROMBOPAG OLAMINEEQ 25MG ACIDTABLET / ORALAB2026-04-28caaa826d4ba7…
2026-08-18 06:07:402026-07A220660-003ELTROMBOPAG OLAMINEEQ 50MG ACIDTABLET / ORALAB2026-04-28caaa826d4ba7…
2026-08-18 06:07:402026-07A220660-004ELTROMBOPAG OLAMINEEQ 75MG ACIDTABLET / ORALAB2026-04-28caaa826d4ba7…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A220660-001ELTROMBOPAG OLAMINEEQ 12.5MG ACIDTABLET / ORALAB2026-04-28a50c72e98297…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A220660-002ELTROMBOPAG OLAMINEEQ 25MG ACIDTABLET / ORALAB2026-04-28a50c72e98297…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A220660-003ELTROMBOPAG OLAMINEEQ 50MG ACIDTABLET / ORALAB2026-04-28a50c72e98297…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A220660-004ELTROMBOPAG OLAMINEEQ 75MG ACIDTABLET / ORALAB2026-04-28a50c72e98297…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2026-09-14 22:38:342026-08A220660-001AB184e616aacf4f…
2026-09-14 22:38:342026-08A220660-002AB184e616aacf4f…
2026-09-14 22:38:342026-08A220660-003AB184e616aacf4f…
2026-09-14 22:38:342026-08A220660-004AB184e616aacf4f…
2026-08-18 06:07:402026-07A220660-001AB1caaa826d4ba7…
2026-08-18 06:07:402026-07A220660-002AB1caaa826d4ba7…
2026-08-18 06:07:402026-07A220660-003AB1caaa826d4ba7…
2026-08-18 06:07:402026-07A220660-004AB1caaa826d4ba7…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A220660-001AB1a50c72e98297…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A220660-002AB1a50c72e98297…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A220660-003AB1a50c72e98297…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A220660-004AB1a50c72e98297…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Eltrombopag
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ELTROMBOPAG OLAMINE12.5 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
4U07F515LGInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
825421Internal RxNorm lookup
825427Internal RxNorm lookup
884617Internal RxNorm lookup
1245001Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
074dbfa7-eadb-e722-0a7a-86a97882f031Available on FDA.report

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
EltrombopagELTROMBOPAGBiocon Pharma Inc.074dbfa7-eadb-e722-0a7a-86a97882f0312025-06-10Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 220660
application number: ANDA220660
ndc (product): 70377-183

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
70377-183-117037701831130 TABLET, FILM COATED in 1 BOTTLE (70377-183-11) 2026-09-09NoNoCurrent