Citalopram Hydrobromide
- Product NDC
- 17856-0540
- 11-digit product format
- 178560540
- Labeler code
- 17856
- Product ID
- 17856-0540_1b2649f2-df2e-4fed-a25a-7df9093103db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Atlantic Biologicals Corps
- Application
- ANDA077629
- Marketing category
- ANDA
- Marketing start
- 2006-06-14
- Marketing end
- 0000-00-00
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 10 mg/5mL
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 17856-0540-2 | Citalopram Hydrobromide | 10 mL in 1 CUP | SOLUTION | 10 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-0540 | CITALOPRAM HYDROBROMIDE SOLUTION [ATLANTIC BIOLOGICALS CORPS] | 2 | Legacy NDC, 1 package rows | 20160504_1f7a3c37-45cc-4274-930d-24019b870311.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 17856-0540-2 | 17856054002 | 10 mL in 1 CUP | 10 ml | Historical |