FDA.reportPublic FDA data

NDC 59762-0075-01 - Hydrocortisone

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
59762-0075
Requested NDC
59762-0075-01
Package NDCs from labels
59762-0075-1, 59762-0075-01
Manufacturer
Mylan Pharmaceuticals Inc. | Pfizer Inc | Pharmacia & Upjohn Company LLC
Effective date
2026-05-25
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Hydrocortisone tablets, USPMylan Pharmaceuticals Inc. | Pfizer Inc | Pharmacia & Upjohn Company LLC2026-05-25HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59762-0075-1Hydrocortisone100 in 1 BOTTLETABLET10012

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59762-0075HYDROCORTISONE TABLET [MYLAN PHARMACEUTICALS INC.]10Current NDC, Legacy NDC, 1 package rows20250523_bc751403-94f2-4f9d-b533-cf6186a40ceb.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59762-0075-1EA - Each59762-0075fb34286f-b583-4003-abf8-e346396869a112013-03-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
HYDROCORTISONEACTIVE INGREDIENTWI4X0X7BPJHYDROCORTISONE TABLET [GREENSTONE LLC]2
HYDROCORTISONEACTIVE MOIETYWI4X0X7BPJHYDROCORTISONE TABLET [GREENSTONE LLC]2
CALCIUM STEARATEINACTIVE INGREDIENT776XM7047LHYDROCORTISONE TABLET [GREENSTONE LLC]2
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GHYDROCORTISONE TABLET [GREENSTONE LLC]2
MINERAL OILINACTIVE INGREDIENTT5L8T28FGPHYDROCORTISONE TABLET [GREENSTONE LLC]2
SORBIC ACIDINACTIVE INGREDIENTX045WJ989BHYDROCORTISONE TABLET [GREENSTONE LLC]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJHYDROCORTISONE TABLET [GREENSTONE LLC]2
SUCROSEINACTIVE INGREDIENTC151H8M554HYDROCORTISONE TABLET [GREENSTONE LLC]2

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 4 of 34 · 666 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HEMORRHOIDALMINERAL, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDECVS PHARMACY, INC93482a9b-145b-42d4-96db-599c281a39f12026-06-10WarningsExact identifier
unii: T5L8T28FGP
good sense anti itchHYDROCORTISONEPreferred Pharmaceuticals Inc.e51047da-8e17-4dd7-be3c-54820a7485f22026-06-09WarningsExact identifier
unii: WI4X0X7BPJ
Walgreens Scalp Itch ReliefHYDROCORTISONEWalgreens34952272-1f9e-c642-e063-6394a90ae2bd2026-05-29WarningsExact identifier
unii: WI4X0X7BPJ
ciprofloxacin hydrochloride and hydrocortisoneCIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONESandoz Incc0881bbe-cc95-45d4-9878-3bc8946eff262026-05-29Warnings, Adverse reactionsExact identifier
unii: WI4X0X7BPJ
HydrocortisoneHYDROCORTISONEMylan Pharmaceuticals Inc.bc751403-94f2-4f9d-b533-cf6186a40ceb2026-05-25Warnings, Adverse reactionsExact identifier
application number: NDA008697
ndc (package): 59762-0073-1
ndc (package): 59762-0075-1
ndc (package): 59762-0074-1
ndc (product): 59762-0075
ndc (product): 59762-0073
ndc (product): 59762-0074
ndc11 (package): 59762007501
rxcui: 197782
rxcui: 197787
rxcui: 197783
spl id: ac03d89e-21e7-4bd4-8355-cafa20808953
spl set id: bc751403-94f2-4f9d-b533-cf6186a40ceb
unii: WI4X0X7BPJ
topcare hydrocortisoneHYDROCORTISONETopco Associates LLC858053a0-d888-4bb9-b94e-503bcf3864cb2026-05-21WarningsExact identifier
unii: WI4X0X7BPJ
HydrocortisoneHYDROCORTISONEBryant Ranch Prepack04758c46-0ca4-4852-acdc-1f8553ce2e6e2026-05-21Adverse reactionsExact identifier
unii: WI4X0X7BPJ
REFRESH LACRI-LUBEMINERAL OIL, PETROLATUMAllergan, Inc.d232a44b-516d-4cdf-a4e7-c3a9a50dc7af2026-05-15WarningsExact identifier
unii: T5L8T28FGP
Scalpicin Anti-Itch Maximum StrengthHYDROCORTISONEReckitt Benckiser LLC7b1a29fa-b266-43e6-a87b-aa3c96ab40412026-05-13WarningsExact identifier
unii: WI4X0X7BPJ
DERMFREE Anti-itch CreamHYDROCORTISONE1% ANTI-ITCH CREAMJiangxi Zhongletang Pharmaceuticals Co.,Ltd.519c319a-9c43-0e63-e063-6394a90ab8692026-05-13WarningsExact identifier
unii: WI4X0X7BPJ
HydrocortisoneHYDROCORTISONEPreferred Pharmaceuticals Inc.02ab1006-c7c8-42c9-bda8-62c9d71425212026-05-11Adverse reactionsExact identifier
unii: WI4X0X7BPJ
HydrocortisoneHYDROCORTISONEPreferred Pharmaceuticals, Inc.058bb2ff-ff51-4a3b-ba47-cb02272d06312026-05-11Adverse reactionsExact identifier
unii: WI4X0X7BPJ
hydrocortisoneHYDROCORTISONEPreferred Pharmaceuticals Inc.12cd35e3-e707-4551-b778-bf615c1a8d322026-05-11WarningsExact identifier
unii: WI4X0X7BPJ
HYDROCORTISONEHYDROCORTISONEPreferred Pharmaceuticals Inc.0bbb8a63-ae1d-41d7-b201-d1b171b31f462026-05-11Warnings, Adverse reactionsExact identifier
rxcui: 197787
unii: WI4X0X7BPJ
HydrocortisoneHYDROCORTISONEPreferred Pharmaceuticals, Inc.026728d4-846b-4bd4-9183-ae6c4a7141382026-05-11Adverse reactionsExact identifier
unii: WI4X0X7BPJ
Harris Teeter HydrocortisoneHYDROCORTISONEHARRIS TEETER LLC4e8199f8-96ec-5342-e063-6294a90afb2d2026-05-07WarningsExact identifier
unii: WI4X0X7BPJ
CAREALL Hydrocortisone Maximum StrengthHYDROCORTISONENew World Imports, Inc.5114cdba-96a1-c399-e063-6294a90aac122026-05-06WarningsExact identifier
unii: WI4X0X7BPJ
hydrocortisoneHYDROCORTISONEPadagis Israel Pharmaceuticals Ltd2dc7f76f-f9ad-46ba-8b41-952e1c15f0522026-04-29WarningsExact identifier
unii: WI4X0X7BPJ
anti itchHYDROCORTISONEHyVee Ince1db3641-2e83-4fec-8394-98d0d876ce0d2026-04-29WarningsExact identifier
unii: WI4X0X7BPJ
FixMySkin Healing Balm Vanilla FlavorHYDROCORTISONELovely Skin, Inc.52f7a561-a0b5-4562-a588-d74fd874b83a2026-04-28WarningsExact identifier
unii: WI4X0X7BPJ

Reported adverse events (FAERS/openFDA)#

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