NDC 68180-999 – Fluoxetine Hydrochloride
Fluoxetine Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC68180-999
Product details
- Brand name
- Fluoxetine Hydrochloride
- Generic name
- Fluoxetine Hydrochloride
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA211653
- Marketed since
- August 7, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Fluoxetine hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68180-999-01 | 100 TABLET in 1 BOTTLE (68180-999-01) | Aug 7, 2019 |
| 68180-999-06 | 30 TABLET in 1 BOTTLE (68180-999-06) | Aug 7, 2019 |
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