Fluoxetine Hydrochloride
- Product NDC
- 60760-282
- 11-digit product format
- 607600282
- Labeler code
- 60760
- Product ID
- 60760-282_7a8e3330-b5b9-2026-e053-2a91aa0a9c23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- St. Marys Medical Park Pharmacy
- Application
- ANDA075049
- Marketing category
- ANDA
- Marketing start
- 2018-04-25
- Marketing end
- 0000-00-00
- Substance
- FLUOXETINE HYDROCHLORIDE
- Active strength
- 20 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-282-90 | 60760028290 | 90 CAPSULE in 1 BOTTLE, PLASTIC (60760-282-90) | 90 capsule | 2018-04-25 | 0000-00-00 | No | No | Current |