NDC 71335-0923 – Fluoxetine
Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral
Product NDC71335-0923
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA204597
- Marketed since
- March 16, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 20 mg/1
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0923-1 | 30 CAPSULE in 1 BOTTLE (71335-0923-1) | Aug 9, 2018 |
| 71335-0923-2 | 100 CAPSULE in 1 BOTTLE (71335-0923-2) | Aug 9, 2018 |
| 71335-0923-3 | 60 CAPSULE in 1 BOTTLE (71335-0923-3) | Aug 9, 2018 |
| 71335-0923-4 | 15 CAPSULE in 1 BOTTLE (71335-0923-4) | Aug 9, 2018 |
| 71335-0923-5 | 56 CAPSULE in 1 BOTTLE (71335-0923-5) | Aug 9, 2018 |
| 71335-0923-6 | 28 CAPSULE in 1 BOTTLE (71335-0923-6) | Aug 9, 2018 |
| 71335-0923-7 | 90 CAPSULE in 1 BOTTLE (71335-0923-7) | Aug 9, 2018 |
| 71335-0923-8 | 120 CAPSULE in 1 BOTTLE (71335-0923-8) | Aug 9, 2018 |
| 71335-0923-9 | 45 CAPSULE in 1 BOTTLE (71335-0923-9) | Aug 9, 2018 |
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