NDC 16729-282 – Aripiprazole
Aripiprazole 20 mg/1 · Tablet · Oral
Product NDC16729-282
Product details
- Brand name
- Aripiprazole
- Generic name
- Aripiprazole
- Labeler
- Accord Healthcare, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA206251
- Marketed since
- February 15, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Atypical Antipsychotic
Active ingredients
- Aripiprazole 20 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 16729-282-01 | 100 TABLET in 1 BOTTLE, PLASTIC (16729-282-01) | Feb 15, 2017 |
| 16729-282-10 | 30 TABLET in 1 BOTTLE, PLASTIC (16729-282-10) | Feb 15, 2017 |
Recalls mentioning this NDC
- D-0370-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0366-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0365-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0367-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0368-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0369-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection.
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- 16729-278 Aripiprazole 2 mg/1 · Tablet · Accord Healthcare, Inc.
- 16729-279 Aripiprazole 5 mg/1 · Tablet · Accord Healthcare, Inc.