Citalopram Hydrobromide
- Product NDC
- 42254-116
- 11-digit product format
- 422540116
- Labeler code
- 42254
- Product ID
- 42254-116_3993eb55-f0e8-496c-a496-19dc509699e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA078216
- Marketing category
- ANDA
- Marketing start
- 2007-10-18
- Marketing end
- 0000-00-00
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 42254-116-60 | Citalopram Hydrobromide | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42254-116 | CITALOPRAM HYDROBROMIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 1 package rows | 20120420_3993eb55-f0e8-496c-a496-19dc509699e8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 42254-116-60 | 42254011660 | 60 in 1 BOTTLE | Historical |