Octreotide Acetate
- Product NDC
- 0480-9259
- 11-digit product format
- 004809259
- Labeler code
- 0480
- Product ID
- 0480-9259_2e77a034-b0ae-4694-8ac0-ae1319754d3a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Octreotide Acetate
- Dosage form
- KIT
- Route
- INTRAMUSCULAR
- Labeler
- Teva Pharmaceuticals, Inc.
- Application
- ANDA210317
- Marketing category
- ANDA
- Marketing start
- 2024-10-01
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Octreotide Acetate
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 898589, 898601, 898605 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0480-9259-08 | Octreotide Acetate | 1 in 1 KIT | KIT | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0480-9259 | OCTREOTIDE ACETATE KIT [TEVA PHARMACEUTICALS, INC.] | 5 | Current NDC, 1 package rows | 20250323_d9739ea6-74de-4a41-a806-6e827a23cedb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0480-9259-08 | 00480925908 | 1 KIT in 1 KIT (0480-9259-08) * 8 mL in 1 VIAL, SINGLE-DOSE (0480-9258-01) * 2 mL in 1 SYRINGE (0480-9263-21) | 1 kit | 2024-10-01 | No | No | Historical |