Citalopram
- Product NDC
- 72162-2567
- 11-digit product format
- 721622567
- Labeler code
- 72162
- Product ID
- 72162-2567_3539e475-18c8-423e-89b3-048879e60f56
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078216
- Marketing category
- ANDA
- Marketing start
- 2007-10-18
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Citalopram
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CITALOPRAM HYDROBROMIDE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I1E9D14F36 |
| Rxcui | 200371 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2567-1 | Citalopram | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 102 |
| 72162-2567-5 | Citalopram | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 102 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2567-1 | 72162256701 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2567-1) | 2007-10-18 | No | No | Historical |
| 72162-2567-5 | 72162256705 | 500 TABLET, FILM COATED in 1 BOTTLE (72162-2567-5) | 2007-10-18 | No | No | Historical |