Citalopram
- Product NDC
- 0185-0372
- 11-digit product format
- 001850372
- Labeler code
- 0185
- Product ID
- 0185-0372_7135ba86-24ce-4783-aebd-1768afcb40a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Eon Labs, Inc.
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0185-0372-01 | 2022-04-13 | C162847 | 48780-1 | 9d75b9d0-be81-f424-e053-dadaa90a57ce | 0979fb90-9c22-4b74-8648-1174b905654d |
| 0185-0372-05 | 2022-04-13 | C162847 | 48780-1 | 9d75b9d0-be81-f424-e053-dadaa90a57ce | 0979fb90-9c22-4b74-8648-1174b905654d |
| 0185-0372-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-be81-f424-e053-dadaa90a57ce | 0979fb90-9c22-4b74-8648-1174b905654d |
| 0185-0372-05 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-be81-f424-e053-dadaa90a57ce | 0979fb90-9c22-4b74-8648-1174b905654d |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0185-0372-01 | EA - Each | 0185-0372 | 7ac7c0c8-07d4-4867-9b72-7893779a4780 | 1 | 2012-07-24 |