FDA.reportPublic FDA data

NDC 72162-2174-01 - Methotrexate

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
72162-2174
Requested NDC
72162-2174-01
Package NDCs from labels
72162-2174-1, 72162-2174-01
Manufacturer
Bryant Ranch Prepack
Effective date
2023-12-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Methotrexate - Bryant Ranch PrepackBryant Ranch Prepack2023-12-07HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-2174-1Methotrexate100 in 1 BOTTLETABLET100100

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-2174METHOTREXATE (METHOTREXATE SODIUM) TABLET [BRYANT RANCH PREPACK]100Current NDC, 1 package rows20231212_c7592288-ac24-46c6-8cec-9abe23d7e81e.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-2174-1EA - Each72162-21743e7668a2-c8de-4e07-83d9-42927167e28012024-02-14

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 2 of 3 · 41 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MethotrexateMETHOTREXATEGolden State Medical Supply, Inc.6f14ced9-c16b-905a-e053-2a91aa0a031e2026-04-15Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 105585
unii: 3IG1E710ZN
MethotrexateMETHOTREXATESafecor Health LLCf177e6fa-c482-432d-8208-937468ab3f102026-01-30Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 105585
unii: 3IG1E710ZN
MethotrexateMETHOTREXATEAvPAK4992fdaa-b880-ee25-e063-6394a90af03b2026-01-29Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 105585
MethotrexateMETHOTREXATEChartwell RX, LLC2609da8f-80dc-448e-8eba-35d11488ce7f2025-12-17Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 105585
unii: 3IG1E710ZN
RasuvoMETHOTREXATEMedexus Pharma Inc.d0075461-0e7e-4967-9c9b-d6440e912c0e2025-12-15Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 3IG1E710ZN
MethotrexateMETHOTREXATEHospira, Inc.0e30eaef-5a09-4104-8a11-c32933eadeab2025-08-22Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 3IG1E710ZN
MethotrexateMETHOTREXATE SODIUMFresenius Kabi USA, LLCec476b11-0b3c-4139-b1eb-a3daa76bc2712025-08-19Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 3IG1E710ZN
MethotrexateMETHOTREXATEMylan Institutional Inc.8df0780e-0fbd-4ab8-80b0-7a5eaa08ec0a2025-07-22Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 105585
unii: 3IG1E710ZN
MethotrexateMETHOTREXATETeva Parenteral Medicines, Inc.346ec9ce-dc98-4a55-b55e-d3af11f2d7032025-07-15Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 3IG1E710ZN
METHOTREXATEMETHOTREXATEEugia US LLC63bb6fbf-dd59-4edc-af8f-d0c397ca12622025-07-10Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 3IG1E710ZN
MethotrexateMETHOTREXATEHospira, Inc.bd287e89-32f9-4396-95fa-4b562869f4762025-06-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 3IG1E710ZN
MethotrexateMETHOTREXATEHospira, Inc.0d63ba29-b692-41b4-87e8-351265c8273f2025-06-10Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 3IG1E710ZN
YVTYVT MICRODERMABRASION FACIAL SCRUBYVTYVT MICRODERMABRASION FACIAL SCRUBBeijing JUNGE Technology Co., Ltd.2f30fc45-42e2-c766-e063-6394a90a8d682025-02-28WarningsExact identifier
unii: OP1R32D61U
MethotrexateMETHOTREXATECoupler LLC2f20d43e-a4b3-a839-e063-6394a90ace382025-02-27Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 105585
unii: 3IG1E710ZN
MethotrexateMETHOTREXATENuCare Pharmaceuticals, Inc.2b61822e-b488-5eaf-e063-6394a90a2dcd2025-01-14Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 105585
unii: 3IG1E710ZN
MethotrexateMETHOTREXATEZydus Lifesciences Limited59ea7b32-2b6d-4197-92c3-015936f04ebe2024-12-05Exact identifier
rxcui: 105585
MethotrexateMETHOTREXATEBryant Ranch Prepacke6611304-4622-4b2e-9b94-57fbad023ae22024-10-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 105585
unii: 3IG1E710ZN
MethotrexateMETHOTREXATEProficient Rx LPa76808f0-38a7-4b54-a4fb-3584f9058ae52024-08-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 105585
unii: 3IG1E710ZN
METHOTREXATEMETHOTREXATEAlembic Pharmaceuticals Limitedff55c573-dc84-4ff3-9d10-2b24c47dd6792024-06-07Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 105585
unii: 3IG1E710ZN
MethotrexateMETHOTREXATE SODIUMBryant Ranch Prepackc7592288-ac24-46c6-8cec-9abe23d7e81e2023-12-07Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA201749
ndc (package): 72162-2174-1
ndc (product): 72162-2174
ndc11 (package): 72162217401
rxcui: 105585
spl id: 2a3d5064-e336-459f-b0dc-28e50256b32e
spl set id: c7592288-ac24-46c6-8cec-9abe23d7e81e
unii: 3IG1E710ZN

Reported adverse events (FAERS/openFDA)#

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