Novolin
- Product NDC
- 50090-0497
- 11-digit product format
- 500900497
- Labeler code
- 50090
- Product ID
- 50090-0497_e4a93fc0-9785-4f8b-b9a8-6c080a310e7d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Human Insulin
- Dosage form
- INJECTION, SOLUTION
- Route
- SUBCUTANEOUS
- Labeler
- A-S Medication Solutions
- Application
- BLA019938
- Marketing category
- BLA
- Marketing start
- 1991-06-25
- Marketing end
- 0000-00-00
- Substance
- INSULIN HUMAN
- Active strength
- 100 [iU]/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0497-0 | 50090049700 | 1 VIAL in 1 CARTON (50090-0497-0) > 10 mL in 1 VIAL | 1 vial | 2014-11-28 | 0000-00-00 | No | No | Current |