NDC 62332-098 – Aripiprazole
Aripiprazole 5 mg/1 · Tablet · Oral
Product NDC62332-098
Product details
- Brand name
- Aripiprazole
- Generic name
- Aripiprazole
- Labeler
- Alembic Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202101
- Marketed since
- July 7, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Aripiprazole 5 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 62332-098-10 | 100 TABLET in 1 CARTON (62332-098-10) | Jul 7, 2016 |
| 62332-098-30 | 30 TABLET in 1 BOTTLE (62332-098-30) | Jul 7, 2016 |
| 62332-098-31 | 100 TABLET in 1 BOTTLE (62332-098-31) | Jul 7, 2016 |
| 62332-098-71 | 500 TABLET in 1 BOTTLE (62332-098-71) | Jul 7, 2016 |
| 62332-098-91 | 1000 TABLET in 1 BOTTLE (62332-098-91) | Jul 7, 2016 |
Recalls mentioning this NDC
- D-1341-2020 Jul 1, 2020 · Class II
Labeling: Label mix up: Bottles labeled as aripiprazole 2 mg, 30 count had aripiprazole 5 mg tablets, 100 count.
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