Sandostatin LAR Depot
- Product NDC
- 0078-0648
- 11-digit product format
- 000780648
- Labeler code
- 0078
- Product ID
- 0078-0648_e969d28c-4f55-4a8f-adb5-078af40c02db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- octreotide acetate
- Dosage form
- KIT
- Labeler
- Novartis Pharmaceuticals
- Application
- NDA021008
- Marketing category
- NDA
- Marketing start
- 2015-02-01
- Marketing end
- 2019-03-31
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0078-0648-61 | EA - Each | 0078-0648 | 8069cdff-a697-470a-b663-cfd8b03b2527 | 1 | 2015-05-05 |
| 0078-0648-81 | EA - Each | 0078-0648 | 5e1b6083-efd0-443e-ab19-fa3ce1c8851f | 1 | 2015-05-05 |