Fluoxetine Hydrochloride
- Product NDC
- 70518-0769
- 11-digit product format
- 705180769
- Labeler code
- 70518
- Product ID
- 70518-0769_8e7e3174-1ab4-b562-e053-2995a90a928a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075049
- Marketing category
- ANDA
- Marketing start
- 2017-10-09
- Marketing end
- 0000-00-00
- Substance
- FLUOXETINE HYDROCHLORIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record