NDC 0074-0010 - Lupron Depot-PED
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
- 0074-0010
- Package NDCs from labels
- 0074-0010-01
- Manufacturer
- AbbVie Inc.
- Effective date
- 2025-11-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Lupron Depot-PED - AbbVie Inc. | AbbVie Inc. | 2025-11-14 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| LEUPROLIDE ACETATE | ACTIVE INGREDIENT | 37JNS02E7V | LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.] | 36 | |
| LEUPROLIDE | ACTIVE MOIETY | EFY6W0M8TG | LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.] | 36 | |
| ACETIC ACID | INACTIVE INGREDIENT | Q40Q9N063P | LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.] | 36 | |
| CARBOXYMETHYLCELLULOSE SODIUM | INACTIVE INGREDIENT | K679OBS311 | LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.] | 36 | |
| ISOPROPYL ALCOHOL | INACTIVE INGREDIENT | ND2M416302 | LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.] | 36 | |
| MANNITOL | INACTIVE INGREDIENT | 3OWL53L36A | LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.] | 36 | |
| POLYLACTIDE | INACTIVE INGREDIENT | 459TN2L5F5 | LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.] | 36 | |
| POLYSORBATE 80 | INACTIVE INGREDIENT | 6OZP39ZG8H | LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.] | 36 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.] | 36 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.