NDC 16714-755 – Atomoxetine
Atomoxetine Hydrochloride 10 mg/1 · Capsule · Oral
Product NDC16714-755
Product details
- Brand name
- Atomoxetine
- Generic name
- Atomoxetine
- Labeler
- Northstar Rx LLC
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA079019
- Marketed since
- June 1, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- Norepinephrine Reuptake Inhibitor
Active ingredients
- Atomoxetine Hydrochloride 10 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 16714-755-01 | 30 CAPSULE in 1 BOTTLE (16714-755-01) | Jun 1, 2018 |
Recalls mentioning this NDC
- D-0240-2025 Feb 26, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. - D-0242-2025 Feb 26, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. - D-0239-2025 Feb 26, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. - D-0238-2025 Feb 26, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. - D-0241-2025 Feb 26, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. - D-0244-2025 Feb 26, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. - D-0243-2025 Feb 26, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
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