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 | Type |
|---|---|---|---|
| Hydrocortisone tablets, USP | Mylan Pharmaceuticals Inc. | Pfizer Inc | Pharmacia & Upjohn Company LLC | 2026-05-25 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59762-0075-1 | Hydrocortisone | 100 in 1 BOTTLE | TABLET | 100 | 12 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 59762-0075 | HYDROCORTISONE TABLET [MYLAN PHARMACEUTICALS INC.] | 10 | Current NDC, Legacy NDC, 1 package rows | 20250523_bc751403-94f2-4f9d-b533-cf6186a40ceb.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 59762-0075-1 | EA - Each | 59762-0075 | fb34286f-b583-4003-abf8-e346396869a1 | 1 | 2013-03-03 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| HYDROCORTISONE | ACTIVE INGREDIENT | WI4X0X7BPJ | HYDROCORTISONE TABLET [GREENSTONE LLC] | 2 | |
| HYDROCORTISONE | ACTIVE MOIETY | WI4X0X7BPJ | HYDROCORTISONE TABLET [GREENSTONE LLC] | 2 | |
| CALCIUM STEARATE | INACTIVE INGREDIENT | 776XM7047L | HYDROCORTISONE TABLET [GREENSTONE LLC] | 2 | |
| LACTOSE | INACTIVE INGREDIENT | J2B2A4N98G | HYDROCORTISONE TABLET [GREENSTONE LLC] | 2 | |
| MINERAL OIL | INACTIVE INGREDIENT | T5L8T28FGP | HYDROCORTISONE TABLET [GREENSTONE LLC] | 2 | |
| SORBIC ACID | INACTIVE INGREDIENT | X045WJ989B | HYDROCORTISONE TABLET [GREENSTONE LLC] | 2 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | HYDROCORTISONE TABLET [GREENSTONE LLC] | 2 | |
| SUCROSE | INACTIVE INGREDIENT | C151H8M554 | HYDROCORTISONE 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Signature Care Hydrocortisone | HYDROCORTISONE | Safeway | beefab66-b056-4bf1-b047-0780704ab87e | 2024-10-29 | Warnings | WI4X0X7BPJ |
| Hydrocortisone | HYDROCORTISONE | H E B | 15eb4676-5f6e-4c28-b5b9-4e45412dc37a | 2024-10-29 | Warnings | WI4X0X7BPJ |
| Lactistat | ARSENICUM ALBUM, CALCAREA CARBONICA, COCCULUS INDICUS, GRAPHITES, HYDROFLUORICUM ACIDUM, LACHESIS MUTUS, LACTICUM ACIDUM, RHUS TOX, RUTA GRAVEOLENS, SARCOLACTICUM ACIDUM, SACCHARUM OFFICINALE | Energique, Inc. | 8dcc4a3a-9f21-4a77-ae42-b2c8283a076a | 2024-10-28 | Warnings | C151H8M554 |
| Grain and Seed Antigens | BAMBOO, BARLEY, CORN, COTTON SEED, FLAX SEED (LINUM USITATISSIMUM), MILLET, MILO, OAT, POPPY SEED, RICE, RYE, SAFFLOWER, SESAME, SORGHUM, SOY BEAN, SUGARCANE, SUNFLOWER (HELIANTHUS ANNUUS), WHEAT, ARSENICUM ALBUM, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, SULPHUR | Energique, Inc. | a028eaea-76ef-45db-80e1-d7b4a0655d5e | 2024-10-25 | Warnings | C151H8M554 |
| Monistat Complete Care Instant Itch Relief | HYDROCORTISONE | Insight Pharmaceuticals LLC | a0f40504-6183-4f32-8d17-6586b3f386a6 | 2024-10-25 | Warnings | WI4X0X7BPJ |
| Dermarest Eczema Medicated | HYDROCORTISONE | Insight Pharmaceuticals LLC | 0292ab62-5088-45fa-a056-70c2fcc19ef7 | 2024-10-25 | Warnings | WI4X0X7BPJ |
| anti itch | HYDROCORTISONE | Meijer, Inc. | 2db7bcab-acb8-48ad-8cd1-842ff7765ed9 | 2024-10-23 | Warnings | WI4X0X7BPJ |
| berkley and jensen anti itch | HYDROCORTISONE | BJWC | 5cc6e4f6-c62d-4923-9726-9dbc569a3f49 | 2024-10-19 | Warnings | WI4X0X7BPJ |
| DG Health Hydrocortisone Maximum Strength | HYDROCORTISONE | Dolgencorp Inc | 2cc792b8-dce6-4178-bd6d-63ba268b7747 | 2024-10-19 | Warnings | WI4X0X7BPJ |
| signature care hemorrhoidal | MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL | Safeway | afcf68cf-f187-44d3-ad91-b1e79b182bc6 | 2024-10-17 | Warnings | T5L8T28FGP |
| hemorrhoidal | MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL | Meijer Distribution Inc | 14319ba4-3bce-497c-a380-65bd24defc5d | 2024-10-17 | Warnings | T5L8T28FGP |
| Equate Hemorrhoidal | MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL | Wal-Mart Stores Inc | 81ecb091-38da-4b3e-a0a1-b4986b97ee09 | 2024-10-16 | Warnings | T5L8T28FGP |
| Hemorrhoidal | MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL | Kroger Company | 5c81d564-f786-46e1-af8b-f47521fbae60 | 2024-10-16 | Warnings | T5L8T28FGP |
| topcare hemorrhoidal | MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL | Topco Associates LLC | 615e87e4-79e0-44d6-b563-3bcd5a9b2d93 | 2024-10-16 | Warnings | T5L8T28FGP |
| Basic Care Hemorrhoidal | MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL | Amazon.com Services LLC | fe675174-fc95-4dd7-bd39-c209c6ce0f6c | 2024-10-16 | Warnings | T5L8T28FGP |
| hydrocortisone | HYDROCORTISONE | H E B | 25ec9014-64c4-44df-9e67-9f9223ffc923 | 2024-10-12 | Warnings | WI4X0X7BPJ |
| HYDROCORTISONE | HYDROCORTISONE | VIVE HEALTH LLC | 24221805-e5c9-5785-e063-6394a90a9d2f | 2024-10-10 | Warnings | WI4X0X7BPJ |
| HYDROCORTISONE | HYDROCORTISONE | VIVE HEALTH LLC | 2410dc2f-9332-19fa-e063-6394a90a2835 | 2024-10-09 | Warnings | WI4X0X7BPJ |
| topcare hydrocortisone | HYDROCORTISONE | Topco Associates LLC | 11a30ec9-ebc2-4a00-8a8d-431d0d973b37 | 2024-10-03 | Warnings | WI4X0X7BPJ |
| Good Sense Anti Itch | HYDROCORTISONE | L. Perrigo Company | ecd6d841-40b9-42c9-825d-d172cd04824d | 2024-10-03 | Warnings | WI4X0X7BPJ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.