NDC 0480-9259 – Octreotide Acetate
· Kit · Intramuscular
Product NDC0480-9259
Product details
- Brand name
- Octreotide Acetate
- Generic name
- Octreotide Acetate
- Labeler
- Teva Pharmaceuticals, Inc.
- Dosage form
- Kit
- Route
- Intramuscular
- Marketing category
- ANDA · ANDA210317
- Marketed since
- October 1, 2024
- Listing expires
- December 31, 2026
Active ingredients
Uses, dosage, side effects and warnings for Octreotide Acetate →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0480-9259-08 | 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) | Oct 1, 2024 |
Recalls mentioning this NDC
- D-0519-2026 May 13, 2026 · Class II
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer. - D-0405-2026 Apr 1, 2026 · Class II
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer. - D-0406-2026 Apr 1, 2026 · Class II
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer. - D-0404-2026 Apr 1, 2026 · Class II
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
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