Citalopram
- Product NDC
- 55700-356
- 11-digit product format
- 557000356
- Labeler code
- 55700
- Product ID
- 55700-356_a5765fb0-8f5b-402b-8bfc-e1233785a60e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077031
- Marketing category
- ANDA
- Marketing start
- 2004-10-28
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 55700-356-30 | 2025-01-09 | C162847 | 48780-1 | ba0f9c33-5c43-a910-e053-dadaa90a0b85 | f2d91cb9-b040-4a5e-b0fa-92bf07bc6a0b |
| 55700-356-90 | 2025-01-09 | C162847 | 48780-1 | ba0f9c33-5c43-a910-e053-dadaa90a0b85 | f2d91cb9-b040-4a5e-b0fa-92bf07bc6a0b |
| 55700-356-30 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-5c43-a910-e053-dadaa90a0b85 | f2d91cb9-b040-4a5e-b0fa-92bf07bc6a0b |
| 55700-356-90 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-5c43-a910-e053-dadaa90a0b85 | f2d91cb9-b040-4a5e-b0fa-92bf07bc6a0b |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55700-356-30 | EA - Each | 55700-356 | 75a0d644-4a84-4e4f-ab9f-8e2dfc22aab7 | 1 | 2016-05-16 |
| 55700-356-90 | EA - Each | 55700-356 | bc720163-1b7b-4ba0-8a90-259b6efc41ee | 1 | 2016-05-16 |