NDC 83209-721 – Fluoxetine
Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral
Product NDC83209-721
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine
- Labeler
- Boswell Pharmacy Services LLC d/b/a BPS Wholesale
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA078619
- Marketed since
- May 20, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 20 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 83209-721-06 | 6 CAPSULE in 1 BLISTER PACK (83209-721-06) | May 20, 2024 |
| 83209-721-10 | 10 CAPSULE in 1 BLISTER PACK (83209-721-10) | May 20, 2024 |
| 83209-721-15 | 15 CAPSULE in 1 BLISTER PACK (83209-721-15) | May 20, 2024 |
| 83209-721-20 | 20 CAPSULE in 1 BLISTER PACK (83209-721-20) | May 20, 2024 |
| 83209-721-30 | 30 CAPSULE in 1 BLISTER PACK (83209-721-30) | May 20, 2024 |
| 83209-721-60 | 60 CAPSULE in 1 BLISTER PACK (83209-721-60) | May 20, 2024 |
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