Novolin
- Product NDC
- 68071-1701
- 11-digit product format
- 680711701
- Labeler code
- 68071
- Product ID
- 68071-1701_bb12818d-d70a-b501-e053-2a95a90a7c61
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Human Insulin
- Dosage form
- INJECTION, SOLUTION
- Route
- SUBCUTANEOUS
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
- 2022-12-31
- 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 |
|---|
| 68071-1701-1 | 68071170101 | 10 mL in 1 BOX (68071-1701-1) | 10 ml | 2019-02-07 | 0000-00-00 | No | No | Current |