FDA.reportPublic FDA data

NDC 71335-2901-01 - PROPYLTHIOURACIL

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
71335-2901
Requested NDC
71335-2901-01
Package NDCs from labels
71335-2901-1, 71335-2901-01
Manufacturer
Bryant Ranch Prepack
Effective date
2025-11-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PROPYLTHIOURACIL - Bryant Ranch PrepackBryant Ranch Prepack2025-11-11HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-2901-1PROPYLTHIOURACIL100 in 1 BOTTLETABLET100100

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-2901-1EA - Each71335-290167657612-3146-4653-8bef-d0c2d0bb3b1412026-01-08

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 ยท 14 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PropylthiouracilPROPYLTHIOURACILAmerican Health Packagingd819e532-09ac-434a-84a6-636c4204c7aa2026-08-27Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 198175
unii: 721M9407IY
PropylthiouracilPROPYLTHIOURACILPar Health USA, LLCb0c23a2c-b250-4c0d-9b2a-c1483faa2ca02026-08-25Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 198175
unii: 721M9407IY
Caldesene BabySTARCH, CORN AND ZINC OXIDEInsight Pharmaceuticals LLC9f12dee2-7afa-45e9-a729-0fd42bb777152026-04-22WarningsExact identifier
unii: O8232NY3SJ
Caldesene Medicated ProtectingCORNSTARCH AND ZINC OXIDEInsight Pharmaceuticals LLCffc92a0f-a7cf-4a46-b2f1-089df2bbb96b2026-04-22WarningsExact identifier
unii: O8232NY3SJ
Lotrimin Daily Sweat and Odor ControlTOPICAL STARCHBayer HealthCare LLC.9ec5c80d-b550-496f-e053-2a95a90a54892026-01-16WarningsExact identifier
unii: O8232NY3SJ
Medicated Cornstarch Baby PowderACTIVE CORN STARCHDavion, Inc.e39032d1-c8cd-4a41-af10-126970b8ad382025-12-29WarningsExact identifier
unii: O8232NY3SJ
PROPYLTHIOURACILPROPYLTHIOURACILBryant Ranch Prepacka032648a-a6e4-4356-a483-8eee037790302025-11-11Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA080154
ndc (package): 71335-2901-1
ndc (product): 71335-2901
ndc11 (package): 71335290101
rxcui: 198175
spl id: abe2d5d5-aac6-442a-a2b7-1a6eccd2297b
spl set id: a032648a-a6e4-4356-a483-8eee03779030
unii: 721M9407IY
YVTYVT MICRODERMABRASION FACIAL SCRUBYVTYVT MICRODERMABRASION FACIAL SCRUBBeijing JUNGE Technology Co., Ltd.2f30fc45-42e2-c766-e063-6394a90a8d682025-02-28WarningsExact identifier
unii: OP1R32D61U
PropylthiouracilPROPYLTHIOURACILMacleods Pharmaceuticals Limiteda251e4cb-01f1-4fd8-bd30-362126b850732024-09-20Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 198175
unii: 721M9407IY
PROPYLTHIOURACILPROPYLTHIOURACILBryant Ranch Prepackae65e8b0-91b2-4a3f-8e1a-279e47eee9512024-08-20Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA080154
rxcui: 198175
unii: 721M9407IY
Pure Cornstarch BabyCORN STARCHWalgreen Companyd0e9bd13-b568-4f7e-b036-8d23e71ad8bf2024-03-25WarningsExact identifier
unii: O8232NY3SJ
PropylthiouracilPROPYLTHIOURACILChartwell RX, LLC53c5f586-3e72-479d-89ba-379683c8f6ba2023-12-26Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 198175
unii: 721M9407IY
PropylthiouracilPROPYLTHIOURACILTeva Pharmaceuticals, Inc.804fa92a-a5ba-4be0-aa44-a40a2e89fde62023-07-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 198175
unii: 721M9407IY
PROPYLTHIOURACILPROPYLTHIOURACILQUAGEN PHARMACEUTICALS LLC84eae11a-b572-4570-b288-ac2cdd3741862023-02-15Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA080154
ndc (product): 70752-171
rxcui: 198175
spl id: 4a15d422-7a6a-4b92-a4cf-3632250c9580
spl set id: 84eae11a-b572-4570-b288-ac2cdd374186
unii: 721M9407IY

Reported adverse events (FAERS/openFDA)#

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