NDC 55111-284 – Fluoxetine hydrochloride
Fluoxetine Hydrochloride 90 mg/1 · Capsule, Delayed Release Pellets · Oral
Product NDC55111-284
Product details
- Brand name
- Fluoxetine hydrochloride
- Generic name
- Fluoxetine Hydrochloride
- Labeler
- Dr.Reddy's Laboratories Limited
- Dosage form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing category
- ANDA · ANDA078572
- Marketed since
- March 24, 2010
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 90 mg/1
Uses, dosage, side effects and warnings for Fluoxetine hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 55111-284-48 | 1 BLISTER PACK in 1 CARTON (55111-284-48) / 4 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK | Mar 24, 2010 |
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