NDC 47335-615 – Norepinephrine Bitartrate
Norepinephrine Bitartrate 1 mg/mL · Injection, Solution, Concentrate · Intravenous
Product NDC47335-615
Product details
- Brand name
- Norepinephrine Bitartrate
- Generic name
- Norepinephrine Bitartrate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Marketing category
- ANDA · ANDA211980
- Marketed since
- July 1, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Catecholamine
Active ingredients
- Norepinephrine Bitartrate 1 mg/mL
Uses, dosage, side effects and warnings for Norepinephrine Bitartrate →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 47335-615-44 | 10 VIAL, SINGLE-DOSE in 1 CARTON (47335-615-44) / 4 mL in 1 VIAL, SINGLE-DOSE | Jul 1, 2021 |
Recalls mentioning this NDC
- D-0529-2023 Apr 19, 2023 · Class III
Failed Impurities/Degradation Specifications: Above the specification limits yielded for related substance norepinephrine sulfonic acid impurity during routine product monitoring.
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