NDC 76045-009-01 - Dilaudid
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
- 76045-009
- Requested NDC
- 76045-009-01
- Package NDCs from labels
- 76045-009-96, 76045-009-06, 76045-009-01, 76045-009-11, 76045-009-03, 76045-009-05, 76045-009-00, 76045-009-10
- Manufacturer
- Fresenius Kabi USA, LLC
- Effective date
- 2026-07-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dilaudid - Fresenius Kabi USA, LLC | Fresenius Kabi USA, LLC | 2026-07-15 | HUMAN PRESCRIPTION DRUG LABEL |
| Dilaudid - Fresenius Kabi USA, LLC | Fresenius Kabi USA, LLC | 2021-01-27 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 76045-009-01 | Dilaudid | 1 mL in 1 SYRINGE | INJECTION, SOLUTION | 1 | 5 | |
| 76045-009-06 | Dilaudid | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | 5 | |
| 76045-009-11 | Dilaudid | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | 5 | |
| 76045-009-96 | Dilaudid | 0.5 mL in 1 SYRINGE | INJECTION, SOLUTION | 0.5 | 5 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 76045-009-01 | ML - Milliliter | 76045-009 | 885a74df-96f1-46a0-9a0a-c4fbd3c1a49b | 1 | 2019-08-06 |
| 76045-009-05 | ML - Milliliter | 76045-009 | d4f0b96b-6409-499a-b51f-52d94170ca61 | 1 | 2017-03-06 |
| 76045-009-06 | ML - Milliliter | 76045-009 | faa348d4-5bce-4c74-81fb-9b8761f878bf | 1 | 2019-08-06 |
| 76045-009-10 | ML - Milliliter | 76045-009 | 7fd0df5b-026f-41a4-a582-e391940e2fb9 | 1 | 2017-03-06 |
| 76045-009-11 | ML - Milliliter | 76045-009 | d09772d6-b441-49ba-bd76-78d2dd814949 | 1 | 2019-08-06 |
| 76045-009-96 | ML - Milliliter | 76045-009 | 1530eb8e-99d1-4f20-af3f-48166d4a1e32 | 1 | 2019-08-06 |
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 |
|---|---|---|---|---|---|---|
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Teva Parenteral Medicines, Inc. | f0b78db9-a38c-41bb-8233-5e93f7f18c5c | 2026-05-14 | Boxed warning, Warnings, Adverse reactions | L960UP2KRW |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Rhodes Pharmaceuticals LLC | 37565441-0d95-4743-a695-d7b3326f58a1 | 2026-05-14 | Boxed warning, Warnings, Adverse reactions | L960UP2KRW |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | American Health Packaging | fab97112-e276-40e0-bc82-0a29d7fa75fa | 2026-05-12 | Boxed warning, Warnings, Adverse reactions | L960UP2KRW |
| Sterile Water | WATER | Hospira, Inc. | 3a6422e1-feee-4095-8883-2b0837039e6e | 2026-05-07 | Warnings, Adverse reactions | 059QF0KO0R |
| Multi Flower | AESCULUS CARNEA, FLOS, AESCULUS HIPPOCASTANUM, FLOS, AGRIMONIA EUPATORIA, FLOS, BROMUS RAMOSUS, FLOS, CALLUNA VULGARIS, FLOS, CARPINUS BETULUS , FLOS, CASTANEA SATIVA, FLOS, CENTAURIUM UMBELLATUM, FLOS, CERATOSTIGMA WILLMOTTIANUM, FLOS, CICHORIUM INTYBUS, FLOS, CLEMATIS VITALBA, FLOS, CLEMATIS VITALBA, FLOS, FAGUS SYLVATICA, FLOS, GENTIANELLA AMARELLA, FLOS, HELIANTHEMUM NUMMULARIUM, FLOS, ILEX AQUIFOLIUM, FLOS, IMPATIENS GLANDULIFERA, FLOS, LARIX DECIDUA, FLOS, LONICERA CAPRIFOLIUM, FLOS | Energique, Inc. | 09c059e7-f748-402c-8447-af5b61169c58 | 2026-05-06 | Warnings | 059QF0KO0R |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Hospira, Inc. | 3832ede8-d3fc-455d-ecab-3b77be5869f5 | 2026-04-21 | Boxed warning, Warnings, Adverse reactions | L960UP2KRW |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Bryant Ranch Prepack | c48e2e9a-cb5b-46b8-b6be-3dd76e80d0ca | 2026-04-10 | Boxed warning, Warnings, Adverse reactions | L960UP2KRW |
| Sodium Citrate and Citric Acid | SODIUM CITRATE AND CITRIC ACID | Chartwell Governmental & Specialty RX, LLC | 58c24504-47de-487a-ab8d-18add155ea95 | 2026-04-07 | Adverse reactions | 2968PHW8QP 1Q73Q2JULR |
| KIDS TOOTHPASTE, FOR CAVITY PROTECTION | KIDS TOOTHPASTE FOR CAVITY PROTECTION | Shulisa (Foshan) Daily ChemicalIndustry Co., Ltd | 4e8fab9e-f05c-5e2f-e063-6294a90aecf9 | 2026-04-03 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Hospira, Inc. | 2b9ea23a-f9e9-48a8-25b7-519e3bbd6828 | 2026-03-18 | Warnings, Adverse reactions | 059QF0KO0R |
| TINTED SUNSCREEN FOUNDATION | TINTED SUNSCREEN FOUNDATION | Guanghzou AiXin Biotech Co Ltd | 396393c4-b50c-3877-e063-6294a90a0e9b | 2026-03-17 | Warnings | 059QF0KO0R |
| 2-Pack Facial Serum | 2-PACK FACIAL SERUM | Guangzhou Ariel Biotech Co., Ltd. | 27c7f645-cfb3-6db1-e063-6394a90a42ff | 2026-03-06 | Warnings | 059QF0KO0R |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Hikma Pharmaceuticals USA Inc. | b325028e-0722-4c8c-9fdb-ab6fb0dc460c | 2026-03-02 | Warnings, Adverse reactions | L960UP2KRW |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | American Health Packaging | e4758743-9b2c-4612-8399-ad2db372e2b7 | 2026-02-27 | Boxed warning, Warnings, Adverse reactions | L960UP2KRW |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Hikma Pharmaceuticals USA Inc. | cc574063-6ede-4da7-82c4-7450c92b229b | 2026-02-27 | Boxed warning, Warnings, Adverse reactions | L960UP2KRW |
| Tricitrates | TRICITRATES | Chartwell Governmental & Specialty RX, LLC. | c4ff0407-3930-4c48-afd4-d2cb3e1b18f4 | 2026-02-25 | Warnings, Adverse reactions | 2968PHW8QP 1Q73Q2JULR |
| Potassium Citrate and Citric Acid | POTASSIUM CITRATE AND CITRIC ACID | Chartwell Governmental & Specialty RX, LLC. | fd57a176-7faf-4053-b348-6ba5f192f05a | 2026-02-25 | Warnings, Adverse reactions | 2968PHW8QP |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Hospira, Inc. | f9ca2ef5-46d8-475a-a26e-f7c8becd6db7 | 2026-02-04 | Boxed warning, Warnings, Adverse reactions | 1433251 897756 897757 L960UP2KRW |
| Additive Formula 3 | DEXTROSE MONOHYDRATE, TRISODIUM CITRATE DIHYDRATE, SODIUM CHLORIDE, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE, CITRIC ACID MONOHYDRATE, AND ADENINE | Terumo BCT, Ltd | 9a5247a1-cc05-442d-b2d0-950f887f03c2 | 2026-01-30 | Warnings, Adverse reactions | 2968PHW8QP |
| Sodium Citrate and Citric Acid | SODIUM CITRATE AND CITRIC ACID MONOHYDRATE | Atlantic Biologicals Corp. | 42d837ae-2578-46df-92d2-24774964aaad | 2026-01-28 | Adverse reactions | 1Q73Q2JULR |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.