NDC 71205-975 – Fluoxetine
Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral
Product NDC71205-975
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine Hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA204597
- Marketed since
- September 25, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 20 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71205-975-00 | 100 CAPSULE in 1 BOTTLE (71205-975-00) | May 7, 2020 |
| 71205-975-11 | 1000 CAPSULE in 1 BOTTLE (71205-975-11) | May 7, 2020 |
| 71205-975-30 | 30 CAPSULE in 1 BOTTLE (71205-975-30) | May 7, 2020 |
| 71205-975-55 | 500 CAPSULE in 1 BOTTLE (71205-975-55) | May 7, 2020 |
| 71205-975-60 | 60 CAPSULE in 1 BOTTLE (71205-975-60) | May 7, 2020 |
| 71205-975-72 | 120 CAPSULE in 1 BOTTLE (71205-975-72) | May 7, 2020 |
| 71205-975-90 | 90 CAPSULE in 1 BOTTLE (71205-975-90) | May 7, 2020 |
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