Citalopram
- Product NDC
- 53217-191
- 11-digit product format
- 532170191
- Labeler code
- 53217
- Product ID
- 53217-191_91d353d1-48e3-4b84-8e33-4fac37f52464
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA077534
- Marketing category
- ANDA
- Marketing start
- 2016-07-22
- 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
- 2019-12-31
- 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 |
|---|
| 53217-191-30 | Citalopram | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 53217-191-60 | Citalopram | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
| 53217-191-90 | Citalopram | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-191 | CITALOPRAM TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 3 package rows | 20170422_09ef1fed-8f7c-49e9-b53c-3f39b0071c69.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-191-30 | 53217019130 | 30 in 1 BOTTLE | Historical |
| 53217-191-60 | 53217019160 | 60 in 1 BOTTLE | Historical |
| 53217-191-90 | 53217019190 | 90 in 1 BOTTLE | Historical |