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 |
|---|---|---|---|---|---|---|
| KUGIG ALOE FOAMING INTIMATE WASH | INTIMATE CLEANSING FOAM | Hong Kong KangXing Centennial Management Limited | 59f4d398-1186-a168-e063-6294a90ab44b | 2026-08-26 | Warnings | 059QF0KO0R |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Redpharm Drug | 59d88866-e1ba-9d97-e063-6394a90a7b27 | 2026-08-25 | Boxed warning, Warnings, Adverse reactions | L960UP2KRW |
| Sterile Water | WATER | REMEDYREPACK INC. | 5dd5d148-6e23-41de-bff5-551b2aea9598 | 2026-08-24 | Warnings, Adverse reactions | 059QF0KO0R |
| BM BM63 DROPS | CEANOTHUS, KALI ARSEN, KALI MUR, SELENIUM, THALLIUM, WIESBADEN | BM Private Limited | 59006d82-610a-2e08-e063-6394a90af1ed | 2026-08-14 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Cardinal Health 107, LLC | 48d75a7c-8329-48a8-bea0-a8c144ddf637 | 2026-08-07 | Warnings, Adverse reactions | 059QF0KO0R |
| Garzulys | INSULIN ASPART-FSAN | Meitheal Pharmaceuticals Inc. | 30c64769-d2f7-4604-ac9e-2a6bc09506c9 | 2026-07-31 | Warnings, Adverse reactions | 059QF0KO0R |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Hikma Pharmaceuticals USA Inc. | 67e79859-4efc-4ea7-8211-cadf746bc864 | 2026-07-30 | Boxed warning, Warnings, Adverse reactions | L960UP2KRW |
| DECONIMO Reconstitution | DECONIMO RECONSTITUTION | Image Amazon LLC | 57ab9b1c-9a18-3786-e063-6394a90a2c63 | 2026-07-28 | Warnings | 059QF0KO0R |
| IDkit HP ONE | CITRIC ACID ANHYDROUS AND 13C UREA | Meridian Bioscience Israel Ltd | 8baab7a7-5d20-46ad-9c4a-762992ef6b51 | 2026-07-28 | Warnings, Adverse reactions | 2968PHW8QP |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Hikma Pharmaceuticals USA Inc. | 31d5a37a-0e90-4e88-be14-75c877be9de2 | 2026-07-24 | Boxed warning, Warnings, Adverse reactions | 1433251 2277368 897756 897757 L960UP2KRW |
| Sterile Water | WATER | Cardinal Health 107, LLC | 9655cd02-82b5-4a75-813b-854b19551481 | 2026-07-21 | Warnings, Adverse reactions | 059QF0KO0R |
| Dilaudid | HYDROMORPHONE HYDROCHLORIDE | Fresenius Kabi USA, LLC | 9eebd88a-5632-460f-b7b6-26c8a180540d | 2026-07-15 | Boxed warning, Warnings, Adverse reactions | NDA019034 76045-121-01 76045-009-01 76045-009-96 76045-010-01 76045-010-11 76045-009-11 76045-009-06 76045-121-11 76045-009 76045-121 76045-010 76045000901 2277370 1872265 1433251 1872269 2277368 897756 897757 1872752 002d5650-24df-4b60-a5ce-e7adc091026f 9eebd88a-5632-460f-b7b6-26c8a180540d L960UP2KRW |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | Fresenius Kabi USA, LLC | e034eb96-03e0-46e1-8b92-5e1f94555e7b | 2026-07-15 | Boxed warning, Warnings, Adverse reactions | NDA019034 L960UP2KRW |
| Dr. Drop NMN Vital Balance (Drop No.1 Cream 90g) | NMN (NICOTINAMIDE MONONUCLEOTIDE), ECTOIN (ECTOINE) | Reedfresh Co., LTD | 55d703ca-ff9d-0dbc-e063-6294a90ab6b1 | 2026-07-05 | Warnings | 059QF0KO0R |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Protective Industrial Products, Inc. | 558e5926-9027-d3f6-e063-6294a90ab121 | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 2000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a1d07e-0006-0c75-e063-6394a90a7acc | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 1000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a2f4da-bb1e-8ead-e063-6394a90af72e | 2026-07-02 | Warnings | 059QF0KO0R |
| Sterile Eyesaline Eyewash | STERILE EYESALINE EYEWASH | Protective Industrial Products, Inc. | 55a290e8-8310-8be4-e063-6394a90abdce | 2026-07-02 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Protective Industrial Products, Inc. | 55a261c2-725d-6765-e063-6294a90a3260 | 2026-07-02 | Warnings | 059QF0KO0R |
| Hydromorphone Hydrochloride | HYDROMORPHONE HYDROCHLORIDE | SpecGx LLC | 4c5c1cc8-c42b-46e3-ad68-8e22f57101f2 | 2026-07-02 | Boxed warning, Warnings, Adverse reactions | L960UP2KRW |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.