NDC 68462-266 – Atomoxetine
Atomoxetine Hydrochloride 18 mg/1 · Capsule · Oral
Product NDC68462-266
Product details
- Brand name
- Atomoxetine
- Generic name
- Atomoxetine
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA079019
- Marketed since
- May 30, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Norepinephrine Reuptake Inhibitor
Active ingredients
- Atomoxetine Hydrochloride 18 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68462-266-23 | 2000 CAPSULE in 1 BOTTLE (68462-266-23) | May 30, 2017 |
| 68462-266-30 | 30 CAPSULE in 1 BOTTLE (68462-266-30) | May 30, 2017 |
Recalls mentioning this NDC
- D-0232-2025 Feb 26, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. - D-0235-2025 Feb 26, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. - D-0236-2025 Feb 26, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. - D-0231-2025 Feb 26, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. - D-0233-2025 Feb 26, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. - D-0234-2025 Feb 26, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. - D-0237-2025 Feb 26, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
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