Citalopram
- Product NDC
- 50090-7039
- 11-digit product format
- 500907039
- Labeler code
- 50090
- Product ID
- 50090-7039_c28df410-62de-435b-b371-46b9130a831e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077031
- Marketing category
- ANDA
- Marketing start
- 2004-10-28
- 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 |
|---|
| 50090-7039-0 | Citalopram | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 12 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7039 | CITALOPRAM (CITALOPRAM HYDROBROMIDE) TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 12 | Current NDC, 1 package rows | 20240822_b244d4eb-8311-4663-8bca-dc08e88e5f5d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7039-0 | 50090703900 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7039-0) | 2024-01-11 | No | No | Current |