NDC 0641-6177 – Octreotide Acetate
Octreotide Acetate 200 ug/mL · Injection, Solution · Intravenous, Subcutaneous
Product NDC0641-6177
Product details
- Brand name
- Octreotide Acetate
- Generic name
- Octreotide Acetate
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Injection, Solution
- Route
- Intravenous, Subcutaneous
- Marketing category
- ANDA · ANDA076330
- Marketed since
- April 8, 2005
- Listing expires
- December 31, 2027
- Pharmacologic class
- Somatostatin Analog
Active ingredients
- Octreotide Acetate 200 ug/mL
Uses, dosage, side effects and warnings for Octreotide Acetate →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0641-6177-01 | 1 VIAL, MULTI-DOSE in 1 CARTON (0641-6177-01) / 5 mL in 1 VIAL, MULTI-DOSE | Apr 8, 2005 |
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