HUMATROPE
- Product NDC
- 0002-7335
- 11-digit product format
- 000027335
- Labeler code
- 0002
- Product ID
- 0002-7335_d58db9ae-697e-469c-918d-5fe287a04994
- 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
- 1987-04-01
- Marketing end
- 2021-09-30
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0002-7335-11 | 00002733511 | 1 KIT in 1 CARTON (0002-7335-11) * 5 mL in 1 VIAL (0002-7349-01) * 5 mL in 1 VIAL (0002-7336-01) | 1 kit | 1987-04-01 | 0000-00-00 | No | No | Current |