Fluoxetine
- Product NDC
- 17224-174
- 11-digit product format
- 172240174
- Labeler code
- 17224
- Product ID
- 17224-174_1661c5e0-7a8b-431e-e063-6294a90a434b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLUOXETINE HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Calvin Scott & Co., Inc.
- Application
- ANDA204597
- Marketing category
- ANDA
- Marketing start
- 2015-03-16
- Substance
- FLUOXETINE HYDROCHLORIDE
- Active strength
- 20 mg/1
- 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/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I9W7N6B1KJ |
| Rxcui | 310385 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17224-174-21 | Fluoxetine | 21 in 1 BOTTLE, PLASTIC | CAPSULE | 21 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17224-174 | FLUOXETINE (FLUOXETINE HYDROCHLORIDE) CAPSULE [CALVIN SCOTT & CO., INC.] | 1 | Current NDC, 1 package rows | 20240424_4915e22f-cecb-4261-8389-9bb417a20e82.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 17224-174-21 | 17224017421 | 21 CAPSULE in 1 BOTTLE, PLASTIC (17224-174-21) | 21 capsule | 2015-03-16 | No | No | Current |