NDC 46708-243 – Fluoxetine Hydrochloride
Fluoxetine Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral
Product NDC46708-243
Product details
- Brand name
- Fluoxetine Hydrochloride
- Generic name
- Fluoxetine Hydrochloride
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208698
- Marketed since
- April 15, 2017
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 46708-243-30 | 30 TABLET, FILM COATED in 1 BOTTLE (46708-243-30) | Apr 15, 2017 |
| 46708-243-31 | 100 TABLET, FILM COATED in 1 BOTTLE (46708-243-31) | Apr 15, 2017 |
| 46708-243-91 | 1000 TABLET, FILM COATED in 1 BOTTLE (46708-243-91) | Apr 15, 2017 |
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