Insulin Lispro
- Product NDC
- 66733-822
- 11-digit product format
- 667330822
- Labeler code
- 66733
- Product ID
- 66733-822_19e48f5d-011c-427c-ad08-1ec22626361f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Insulin lispro
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- ImClone LLC
- Application
- BLA020563
- Marketing category
- BLA
- Marketing start
- 2019-03-04
- Marketing end
- 0000-00-00
- Substance
- INSULIN LISPRO
- Active strength
- 100 [iU]/mL
- Pharmacologic classes
- Insulin [Chemical/Ingredient],Insulin Analog [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 66733-822-59 | 66733082259 | 5 SYRINGE in 1 CARTON (66733-822-59) > 3 mL in 1 SYRINGE (66733-822-01) | 5 syringe | 2019-03-19 | 0000-00-00 | No | No | Current |