NDC 67877-432 – Aripiprazole
Aripiprazole 10 mg/1 · Tablet · Oral
Product NDC67877-432
Product details
- Brand name
- Aripiprazole
- Generic name
- Aripiprazole
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207105
- Marketed since
- February 27, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Aripiprazole 10 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 67877-432-01 | 100 TABLET in 1 BOTTLE (67877-432-01) | Feb 27, 2019 |
| 67877-432-03 | 30 TABLET in 1 BOTTLE (67877-432-03) | Feb 27, 2019 |
| 67877-432-05 | 500 TABLET in 1 BOTTLE (67877-432-05) | Feb 27, 2019 |
| 67877-432-32 | 1 BLISTER PACK in 1 CARTON (67877-432-32) / 7 TABLET in 1 BLISTER PACK | Feb 27, 2019 |
| 67877-432-38 | 10 BLISTER PACK in 1 CARTON (67877-432-38) / 10 TABLET in 1 BLISTER PACK (67877-432-33) | Feb 27, 2019 |
Recalls mentioning this NDC
- D-0645-2025 Sep 24, 2025 · Class II
Superpotent drug - D-0539-2023 Apr 26, 2023 · Class II
Out of specification (OOS) for Spectroscopic Identification test by IR.
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