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 |
|---|---|---|---|---|---|---|
| INSULIN DILUTING MEDIUM FOR Kirsty | WATER | Biocon Biologics Inc. | 3db1d482-7e1f-aec6-79ef-3f305b4d8277 | 2026-01-20 | Warnings, Adverse reactions | 059QF0KO0R |
| SWISS BLEU Relief-Calm Antimicrobial Skin Cream | LACTOBACILLUS FERMENT LYSATE, LEONTOPODIUM ALPINUM, CALENDULA OFFICINALIS FLOWER EXTRACT, EVENING PRIMROSE FLOWER EXTRACT, CITRIC ACID | Nanjing Hongruixing Biological Technology Co., Ltd | 487d3c2c-ce28-f7a1-e063-6294a90a5ec6 | 2026-01-16 | Warnings | 2968PHW8QP |
| Walgreens Sterile Soothing Eye Wash | PURIFIED WATER | Walgreens | a62e3294-abd6-48dc-81b1-62a809bdc968 | 2026-01-14 | Warnings | 059QF0KO0R |
| Plus Rinse Emergency Eyewash | PURIFIED WATER | INNOVATIVE SAFETY SUPPLY INC. | b3f47d26-39e4-4aea-bb92-358def52b652 | 2026-01-08 | Warnings | 059QF0KO0R |
| pH Neutral Emergency Eyewash | WATER | INNOVATIVE SAFETY SUPPLY INC. | 29a1bd1e-d0dd-478f-e063-6394a90ab0aa | 2026-01-08 | Warnings | 059QF0KO0R |
| Eye Clean | EYE WASH | HART Health | 41f53e2e-c2bc-4bf1-a541-3bcb2cf63002 | 2025-12-31 | Warnings | 059QF0KO0R |
| teeth and gums | CALC FLUORICA, CALC PHOS, FERRUM PHOS, KALI PHOS, MAG PHOS, MALUS PUMILA, FLOS, ROCK WATER, ULEX EUROPAEUS, FLOS | Siddha Flower Essences LLC | 926c79d5-d270-4c0d-aca9-b58571c24f3a | 2025-12-31 | Warnings | 059QF0KO0R |
| lung and sinus | CALC PHOS, FERRUM PHOS, GENTIANELLA AMARELLA, FLOS, KALI MUR, KALI PHOS, KALI SULPH, ROCK WATER, ROSE CANINA, FLOS | Siddha Flower Essences LLC | 9f7c949f-21bc-473c-ab8d-24837893fccc | 2025-12-31 | Warnings | 059QF0KO0R |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Hikma Pharmaceuticals USA Inc. | c729424e-e483-4bf8-b86c-ce56636dcffa | 2025-12-31 | Boxed warning, Warnings, Adverse reactions | L960UP2KRW |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Hospira, Inc. | e9c9ef18-7dfc-4322-b2fc-29b934c30f8b | 2025-12-31 | Boxed warning, Warnings, Adverse reactions | 897756 897757 L960UP2KRW |
| Quality Choice Eye Wash | WATER | Chain Drug Marketing Assoc., Inc. | 1fb8a109-351b-7039-e063-6394a90a7311 | 2025-12-30 | Warnings | 059QF0KO0R |
| Rite Aid Eye Wash | PURIFIED WATER | Rite Aid | 28a18e04-d735-a511-e063-6394a90af6bb | 2025-12-30 | Warnings | 059QF0KO0R |
| OCUFRESH | WATER | Optics Laboratory Inc. | b8e477a9-66b9-496b-92fb-3d4bbd7b36b5 | 2025-12-29 | Warnings | 059QF0KO0R |
| Kollourion Eyesalve Eyewash | PURIFIED WATER 98.3% | Miracle Eye Pharmaceuticals | b56d2ab9-169b-b490-e053-2a95a90a80b3 | 2025-12-28 | Warnings | 059QF0KO0R |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Trigen Laboratories, LLC | 8bb81796-6990-40e9-bee4-1f292f91ae99 | 2025-12-25 | Boxed warning, Warnings, Adverse reactions | L960UP2KRW |
| hydromorphone hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Padagis US LLC | 780a2616-0392-4715-bc50-71799bea1957 | 2025-12-22 | Boxed warning, Warnings, Adverse reactions | L960UP2KRW |
| Sterile Cord Blood Collection Unit (MSC128D) | ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE SOLUTION | Maco Productions | 251fd4cb-4aa4-4473-9f89-968da856eb77 | 2025-12-18 | Warnings | 2968PHW8QP 1Q73Q2JULR |
| Sterile Cord Blood Collection Unit (MSC127D) | ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE SOLUTION | Maco Productions | 75a008b2-9666-4bfa-ab18-6d09b43b2215 | 2025-12-18 | Warnings | 2968PHW8QP 1Q73Q2JULR |
| Pall Sterile Cord Blood Collection Unit | STERILE CORD BLOOD COLLECTION UNIT | Global Life Sciences Solutions USA LLC | aa9340b7-cc63-e17d-e053-2a95a90ad4d9 | 2025-12-18 | Warnings | 2968PHW8QP 1Q73Q2JULR |
| Sterile Water | WATER | ProPharma Distribution | 386a0a2f-4ff7-f128-e063-6294a90a7d4d | 2025-12-18 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.