NDC 49884-336 – Fluoxetine hydrochloride
Fluoxetine Hydrochloride 20 mg/1 · Tablet, Coated · Oral
Product NDC49884-336
Product details
- Brand name
- Fluoxetine hydrochloride
- Generic name
- Fluoxetine hydrochloride
- Labeler
- Par Health USA, LLC
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203836
- Marketed since
- August 22, 2016
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 49884-336-01 | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-336-01) | Aug 22, 2016 |
| 49884-336-11 | 30 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-336-11) | Aug 22, 2016 |
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