Citalopram
- Product NDC
- 68071-3034
- 11-digit product format
- 680713034
- Labeler code
- 68071
- Product ID
- 68071-3034_d5932692-d9c9-606d-e053-2a95a90a8cf3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA077289
- Marketing category
- ANDA
- Marketing start
- 2010-04-06
- Marketing end
- 0000-00-00
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 10 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 |
|---|
| 68071-3034-3 | 68071303403 | 30 TABLET in 1 BOTTLE (68071-3034-3) | 30 tablet | 2017-03-03 | 0000-00-00 | No | No | Current |
| 68071-3034-5 | 68071303405 | 15 TABLET in 1 BOTTLE (68071-3034-5) | 15 tablet | 2017-03-03 | 0000-00-00 | No | No | Current |
| 68071-3034-6 | 68071303406 | 60 TABLET in 1 BOTTLE (68071-3034-6) | 60 tablet | 2017-03-03 | 0000-00-00 | No | No | Current |
| 68071-3034-9 | 68071303409 | 90 TABLET in 1 BOTTLE (68071-3034-9) | 90 tablet | 2017-03-03 | 0000-00-00 | No | No | Current |