Fluoxetine
- Product NDC
- 63187-218
- 11-digit product format
- 631870218
- Labeler code
- 63187
- Product ID
- 63187-218_cc4cd573-87f8-452f-98c5-7d46362f9080
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA075872
- Marketing category
- ANDA
- Marketing start
- 2002-01-30
- 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
- 2023-12-31
- 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 |
|---|
| 63187-218-30 | 63187021830 | 30 TABLET, FILM COATED in 1 BOTTLE (63187-218-30) | 2019-01-01 | 0000-00-00 | No | No | Current |