Citalopram Hydrobromide
- Product NDC
- 67046-116
- 11-digit product format
- 670460116
- Labeler code
- 67046
- Product ID
- 67046-116_b808f809-40fa-43c6-a33f-2ec21a293051
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA077044
- Marketing category
- ANDA
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 40 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 |
|---|
| 67046-116-30 | Citalopram Hydrobromide | 30 in 1 BLISTER PACK | TABLET | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-116 | CITALOPRAM HYDROBROMIDE TABLET [CONTRACT PHARMACY SERVICES-PA] | 1 | Legacy NDC, 1 package rows | 20100226_b808f809-40fa-43c6-a33f-2ec21a293051.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67046-116-30 | 67046011630 | 30 in 1 BLISTER PACK | Historical |