Fluoxetine
- Product NDC
- 0093-7188
- 11-digit product format
- 000937188
- Labeler code
- 0093
- Product ID
- 0093-7188_36f18cc3-526a-4448-a4fb-803303acd103
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA075872
- Marketing category
- ANDA
- Marketing start
- 2002-01-30
- Marketing end
- 2023-05-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0093-7188-01 | 00093718801 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-7188-01) | 2019-11-12 | 0000-00-00 | No | No | Current |
| 0093-7188-10 | 00093718810 | 1000 TABLET, FILM COATED in 1 BOTTLE (0093-7188-10) | 2002-01-30 | 0000-00-00 | No | No | Current |
| 0093-7188-56 | 00093718856 | 30 TABLET, FILM COATED in 1 BOTTLE (0093-7188-56) | 2002-01-30 | 0000-00-00 | No | No | Current |