Citalopram Hydrobromide
- Product NDC
- 50436-0916
- 11-digit product format
- 504360916
- Labeler code
- 50436
- Product ID
- 50436-0916_bf14f85a-959b-450d-8f8a-b53d245ea182
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA078216
- Marketing category
- ANDA
- Marketing start
- 2007-10-18
- Marketing end
- 0000-00-00
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-0916-1 | Citalopram Hydrobromide | 28 in 1 BOTTLE | TABLET | 28 | | 7 |
| 50436-0916-2 | Citalopram Hydrobromide | 30 in 1 BOTTLE | TABLET | 30 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0916 | CITALOPRAM HYDROBROMIDE TABLET [UNIT DOSE SERVICES] | 7 | Legacy NDC, 2 package rows | 20181010_6eaa0a4a-3c0f-48ea-bbc7-0f7a2d2dd3b0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0916-1 | 50436091601 | 28 in 1 BOTTLE | Historical |
| 50436-0916-2 | 50436091602 | 30 in 1 BOTTLE | Historical |