Fluoxetine
- Product NDC
- 65862-306
- 11-digit product format
- 658620306
- Labeler code
- 65862
- Product ID
- 65862-306_75e37c2c-4f1b-4660-ae32-0ce8106b12ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluoxetine
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA079209
- Marketing category
- ANDA
- Marketing start
- 2009-03-19
- Substance
- FLUOXETINE HYDROCHLORIDE
- Active strength
- 20 mg/5mL
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fluoxetine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FLUOXETINE HYDROCHLORIDE | 20 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I9W7N6B1KJ |
| Rxcui | 310386 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65862-306-12 | Fluoxetine | 120 mL in 1 BOTTLE, GLASS | SOLUTION | 120 | | 24 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65862-306 | FLUOXETINE SOLUTION [AUROBINDO PHARMA LIMITED] | 24 | Current NDC, Legacy NDC, 1 package rows | 20240124_3195db14-0cae-4b49-9fba-49b869fe92a8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65862-306-12 | 65862030612 | 120 mL in 1 BOTTLE, GLASS (65862-306-12) | 120 ml | 2009-03-19 | 0000-00-00 | No | No | Current |