Fluoxetine Hydrochloride
- Product NDC
- 70934-141
- 11-digit product format
- 709340141
- Labeler code
- 70934
- Product ID
- 70934-141_b8ca62dc-b9e9-48be-e053-2995a90a7fdd
- 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
- 2018-06-27
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-141-30 | 70934014130 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70934-141-30) | 30 capsule | 2018-06-27 | 0000-00-00 | No | No | Current |
| 70934-141-90 | 70934014190 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70934-141-90) | 90 capsule | 2019-05-30 | 0000-00-00 | No | No | Current |