Citalopram
- Product NDC
- 71335-0541
- 11-digit product format
- 713350541
- Labeler code
- 71335
- Product ID
- 71335-0541_50ff719b-aa36-4d71-ac53-729b394029bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077534
- Marketing category
- ANDA
- Marketing start
- 2016-07-22
- Marketing end
- 0000-00-00
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0541-1 | 71335054101 | 30 TABLET in 1 BOTTLE (71335-0541-1) | 30 tablet | 2021-06-03 | 0000-00-00 | No | No | Current |
| 71335-0541-2 | 71335054102 | 40 TABLET in 1 BOTTLE (71335-0541-2) | 40 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0541-3 | 71335054103 | 60 TABLET in 1 BOTTLE (71335-0541-3) | 60 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0541-4 | 71335054104 | 90 TABLET in 1 BOTTLE (71335-0541-4) | 90 tablet | 2021-06-14 | 0000-00-00 | No | No | Current |
| 71335-0541-5 | 71335054105 | 100 TABLET in 1 BOTTLE (71335-0541-5) | 100 tablet | 2022-05-02 | 0000-00-00 | No | No | Current |
| 71335-0541-6 | 71335054106 | 180 TABLET in 1 BOTTLE (71335-0541-6) | 180 tablet | 2022-05-02 | 0000-00-00 | No | No | Current |