Citalopram
- Product NDC
- 68071-3558
- 11-digit product format
- 680713558
- Labeler code
- 68071
- Product ID
- 68071-3558_0dfb11d9-f48e-56ee-e063-6294a90ad256
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- citalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077042
- Marketing category
- ANDA
- Marketing start
- 2008-07-28
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 40 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
- Citalopram
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CITALOPRAM HYDROBROMIDE | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I1E9D14F36 |
| Rxcui | 309314 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-3558-1 | Citalopram | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-3558 | CITALOPRAM TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.] | 1 | Current NDC, 1 package rows | 20240103_0dfb11d9-f48d-56ee-e063-6294a90ad256.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3558-1 | 68071355801 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3558-1) | 2024-01-02 | No | No | Current |