Lanreotide Acetate
- Product NDC
- 76282-710
- 11-digit product format
- 762820710
- Labeler code
- 76282
- Product ID
- 76282-710_1eaf1cf6-23b6-4c54-8cbf-a96d1f74c4cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lanreotide acetate
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- Exelan Pharmaceuticals, Inc.
- Application
- NDA215395
- Marketing category
- NDA
- Marketing start
- 2022-06-01
- Marketing end
- 0000-00-00
- Substance
- LANREOTIDE ACETATE
- Active strength
- 90 mg/.3mL
- Pharmacologic classes
- Somatostatin Analog [EPC], Somatostatin Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 76282-710-67 | 76282071067 | 1 SYRINGE in 1 CARTON (76282-710-67) > .3 mL in 1 SYRINGE | 1 syringe | 2022-06-01 | 0000-00-00 | No | No | Current |