HUMATROPE
- Product NDC
- 0002-8149
- 11-digit product format
- 000028149
- Labeler code
- 0002
- Product ID
- 0002-8149_65052345-9f7f-4580-8cff-1e61a421843c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Somatropin
- Dosage form
- KIT
- Route
- INTRAMUSCULAR; SUBCUTANEOUS
- Labeler
- Eli Lilly and Company
- Application
- BLA019640
- Marketing category
- BLA
- Marketing start
- 2006-01-27
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- HUMATROPE
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 582969, 582971, 582974, 582976, 729232, 729234 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0002-7556-01 | HUMATROPE | 2.88 mL in 1 CARTRIDGE | INJECTION, POWDER, FOR SOLUTION | 2.88 mL | 24 mg in 2.88mL | 44 |
| 0002-8149-01 | HUMATROPE | 1 in 1 CARTON | KIT | 1 | | 44 |
| 0002-8149-01 | HUMATROPE | 1 in 1 TRAY | KIT | 1 | | 44 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0002-8149 | HUMATROPE (SOMATROPIN) KIT [ELI LILLY AND COMPANY] | 41 | Current NDC, Legacy NDC, 3 package rows | 20241212_a774e1ae-3997-49ee-8b0e-99a2b315d409.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0002-7556-01 | 00002755601 | 2.88 mL in 1 CARTRIDGE | 2.88 ml | | | | | Historical |
| 0002-8149-01 | 00002814901 | 1 TRAY in 1 CARTON (0002-8149-01) / 1 KIT in 1 TRAY * 2.88 mL in 1 CARTRIDGE (0002-7556-01) * 2.88 mL in 1 SYRINGE (0002-7619-01) | 1 tray | 2006-01-27 | 0000-00-00 | No | No | Current |