United States · FDA National Drug Code directory
Aripiprazole
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 43598-970_5be74c47-c62f-40f5-8aad-bd20f8f4cae3
- Product NDC
- 43598-970
- Form
- TABLET
- Composition / generic term
- Aripiprazole
- Labeler
- Dr.Reddys Laboratories Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200316
- Source listing expiry
- 20261231
Source-listed ingredients
- ARIPIPRAZOLE — 30 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BOTTLE (43598-970-05) · 43598-970-05
- 30 TABLET in 1 BOTTLE (43598-970-30) · 43598-970-30
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →