CITALOPRAM is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Direct Rx. The primary component is Citalopram Hydrobromide.
| Product ID | 61919-056_04fe05a8-eae7-4e24-9081-e982e5e08312 |
| NDC | 61919-056 |
| Product Type | Human Prescription Drug |
| Proprietary Name | CITALOPRAM |
| Generic Name | Citalopram |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2015-01-01 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA077032 |
| Labeler Name | DIRECT RX |
| Substance Name | CITALOPRAM HYDROBROMIDE |
| Active Ingredient Strength | 20 mg/1 |
| Pharm Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2015-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA077032 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-08-14 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA077032 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-01-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA077032 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-07-01 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| CITALOPRAM HYDROBROMIDE | 20 mg/1 |
| SPL SET ID: | b4c389f0-0dad-4fec-ad7d-4223528beb35 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0054-0062 | Citalopram | Citalopram |
| 0121-0848 | Citalopram | Citalopram Hydrobromide |
| 0121-1696 | Citalopram | Citalopram Hydrobromide |
| 0185-0371 | Citalopram | Citalopram Hydrobromide |
| 0185-0372 | Citalopram | Citalopram Hydrobromide |
| 0185-0373 | Citalopram | Citalopram Hydrobromide |
| 0378-6231 | Citalopram | citalopram |
| 0378-6232 | Citalopram | citalopram |
| 0378-6233 | Citalopram | citalopram |
| 0615-6510 | Citalopram | Citalopram |
| 0615-6511 | Citalopram | Citalopram |
| 0615-6512 | Citalopram | Citalopram |
| 0615-8022 | Citalopram | Citalopram Hydrobromide |
| 0615-8023 | Citalopram | Citalopram Hydrobromide |
| 0615-8141 | Citalopram | Citalopram Hydrobromide |
| 0713-4740 | Citalopram | Citalopram Tablets |
| 0713-4741 | Citalopram | Citalopram Tablet |
| 68071-1970 | Citalopram | Citalopram |
| 68071-3042 | Citalopram | Citalopram |
| 68071-3034 | Citalopram | Citalopram |
| 68071-3357 | Citalopram | Citalopram |
| 68071-4291 | Citalopram | Citalopram |
| 68071-4604 | Citalopram | Citalopram |
| 68071-4477 | Citalopram | Citalopram |
| 68071-4324 | Citalopram | Citalopram |
| 68084-737 | Citalopram | Citalopram |
| 68084-744 | Citalopram | Citalopram |
| 68788-6810 | Citalopram | Citalopram |
| 68788-0005 | Citalopram | Citalopram |
| 68788-0007 | Citalopram | Citalopram |
| 69097-822 | Citalopram | Citalopram |
| 69097-824 | Citalopram | Citalopram |
| 69097-823 | Citalopram | Citalopram |
| 70518-0449 | Citalopram | Citalopram |
| 70518-0561 | Citalopram | Citalopram |
| 71335-0541 | Citalopram | Citalopram |
| 71335-0573 | Citalopram | Citalopram |
| 71335-0712 | Citalopram | Citalopram |
| 71335-0656 | Citalopram | Citalopram |
| 0713-4742 | Citalopram | Citalopram |
| 10544-149 | Citalopram | Citalopram |
| 10544-179 | Citalopram | Citalopram |
| 10544-006 | Citalopram | Citalopram |
| 10544-150 | Citalopram | Citalopram |
| 10544-182 | Citalopram | Citalopram |
| 13107-005 | Citalopram | Citalopram |
| 13107-007 | Citalopram | Citalopram |
| 13107-006 | Citalopram | Citalopram |
| 21695-031 | Citalopram | Citalopram |
| 21695-032 | Citalopram | Citalopram |