Citalopram
- Product NDC
- 70518-2671
- 11-digit product format
- 705182671
- Labeler code
- 70518
- Product ID
- 70518-2671_d6e3dc54-cba2-7078-e053-2a95a90a5d43
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- citalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077042
- Marketing category
- ANDA
- Marketing start
- 2020-04-03
- 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
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2671-0 | 70518267100 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2671-0) | 2020-04-03 | 0000-00-00 | No | No | Current |
| 70518-2671-1 | 70518267101 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2671-1) | 2020-04-28 | 0000-00-00 | No | No | Current |