Citalopram Hydrobromide
- Product NDC
- 10544-543
- 11-digit product format
- 105440543
- Labeler code
- 10544
- Product ID
- 10544-543_915057b6-5cd2-4b42-a897-e14aad53561e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Blenheim Pharmacal, Inc.
- Application
- ANDA078216
- Marketing category
- ANDA
- Marketing start
- 2013-10-04
- 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 |
|---|
| 10544-543-30 | Citalopram Hydrobromide | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10544-543 | CITALOPRAM HYDROBROMIDE TABLET [BLENHEIM PHARMACAL, INC.] | 3 | Legacy NDC, 1 package rows | 20150902_645cbf32-4b43-4d09-9935-80bc32b6a6b7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10544-543-30 | 10544054330 | 30 in 1 BOTTLE | Historical |