Citalopram
- Product NDC
- 70518-0561
- 11-digit product format
- 705180561
- Labeler code
- 70518
- Product ID
- 70518-0561_e1e65fe9-8aed-8b00-e053-2995a90a250e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- citalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077042
- Marketing category
- ANDA
- Marketing start
- 2017-06-01
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0561-0 | 70518056100 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0561-0) | 2017-06-01 | 0000-00-00 | No | No | Current |