Citalopram
- Product NDC
- 21695-030
- 11-digit product format
- 216950030
- Labeler code
- 21695
- Product ID
- 21695-030_a0fdcf12-0e79-4814-910f-5f4cc7463c13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rebel Distributors Corp.
- Application
- ANDA078216
- Marketing category
- ANDA
- Marketing start
- 2007-03-27
- 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 |
|---|
| 21695-030-00 | Citalopram | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 2 |
| 21695-030-30 | Citalopram | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 2 |
| 21695-030-60 | Citalopram | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-030 | CITALOPRAM (CITALOPRAM HYDROBROMIDE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 2 | Legacy NDC, 3 package rows | 20100324_b29fab7c-1282-4bb9-a650-24890501caec.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-030-00 | 21695003000 | 100 in 1 BOTTLE | Historical |
| 21695-030-30 | 21695003030 | 30 in 1 BOTTLE | Historical |
| 21695-030-60 | 21695003060 | 60 in 1 BOTTLE | Historical |