Fluoxetine Hydrochloride
- Product NDC
- 70934-394
- 11-digit product format
- 709340394
- Labeler code
- 70934
- Product ID
- 70934-394_ad17951c-b3a7-db92-e053-2995a90a28c5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA075049
- Marketing category
- ANDA
- Marketing start
- 2019-06-17
- Marketing end
- 0000-00-00
- Substance
- FLUOXETINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70934-394-30 | 70934039430 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70934-394-30) | 30 capsule | 2019-06-17 | 0000-00-00 | No | No | Current |