Citalopram
- Product NDC
- 67296-0753
- 11-digit product format
- 672960753
- Labeler code
- 67296
- Product ID
- 67296-0753_9c9b1dc6-f318-f653-e053-2a95a90a6991
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA077534
- Marketing category
- ANDA
- Marketing start
- 2011-01-01
- 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
- 2021-12-31
- 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 |
|---|
| 67296-0753-1 | Citalopram | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 67296-0753-9 | Citalopram | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0753 | CITALOPRAM TABLET [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 2 package rows | 20200121_4183806e-85ed-72f2-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-0753-1 | 67296075301 | 30 TABLET in 1 BOTTLE (67296-0753-1) | 30 tablet | 2011-01-01 | 0000-00-00 | No | No | Current |
| 67296-0753-9 | 67296075309 | 90 TABLET in 1 BOTTLE (67296-0753-9) | 90 tablet | 2011-01-01 | 0000-00-00 | No | No | Current |