Fluoxetine
- Product NDC
- 55700-089
- 11-digit product format
- 557000089
- Labeler code
- 55700
- Product ID
- 55700-089_2d8bb2fd-6585-4fed-935a-9079c6d4e596
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA076001
- Marketing category
- ANDA
- Marketing start
- 2002-01-29
- 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
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 |
|---|
| 55700-089-90 | 55700008990 | 90 CAPSULE in 1 BOTTLE (55700-089-90) | 90 capsule | 2015-09-17 | 0000-00-00 | No | No | Current |