NDC 68645-130 – Fluoxetine
Fluoxetine Hydrochloride 20 mg/1 · Capsule · Oral
Product NDC68645-130
Product details
- Brand name
- Fluoxetine
- Generic name
- Fluoxetine
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA076001
- Marketed since
- January 25, 2011
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Fluoxetine Hydrochloride 20 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68645-130-54 | 30 CAPSULE in 1 BOTTLE (68645-130-54) | Jan 25, 2011 |
Recalls mentioning this NDC
- D-1279-2014 May 7, 2014 · Class II
Chemical Contamination: The recalling firm received notice that their supplier is recalling capsules due to complaints of capsules having an unusual odor.
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