NDC 0121-4721 – Fluoxetine
Fluoxetine Hydrochloride 20 mg/5mL · Solution · Oral
Product NDC0121-4721
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine Hydrochloride
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Dosage form
- Solution
- Route
- Oral
- Marketing category
- ANDA · ANDA076015
- Marketed since
- February 1, 2002
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 20 mg/5mL
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0121-4721-40 | 4 TRAY in 1 CASE (0121-4721-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-4721-05) | Feb 1, 2002 |
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