Fluoxetine
- Product NDC
- 68001-129
- 11-digit product format
- 680010129
- Labeler code
- 68001
- Product ID
- 68001-129_c4f8afaf-f359-7a1f-e053-2995a90a05a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA090223
- Marketing category
- ANDA
- Marketing start
- 2013-12-23
- Marketing end
- 2022-05-31
- 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
- 0000-00-00
- 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 |
|---|
| 68001-129-00 | 68001012900 | 100 CAPSULE in 1 BOTTLE (68001-129-00) | 100 capsule | 2013-12-23 | 0000-00-00 | No | No | Current |
| 68001-129-03 | 68001012903 | 500 CAPSULE in 1 BOTTLE (68001-129-03) | 500 capsule | 2013-12-23 | 0000-00-00 | No | No | Current |
| 68001-129-04 | 68001012904 | 30 CAPSULE in 1 BOTTLE (68001-129-04) | 30 capsule | 2013-12-23 | 0000-00-00 | No | No | Current |