Citalopram Hydrobromide
- Product NDC
- 68645-571
- 11-digit product format
- 686450571
- Labeler code
- 68645
- Product ID
- 68645-571_c599d24a-0982-8c9a-e053-2a95a90a7087
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Application
- ANDA077038
- Marketing category
- ANDA
- Marketing start
- 2004-10-28
- Marketing end
- 2022-11-30
- 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
- 0000-00-00
- 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 |
|---|
| 68645-571-54 | 68645057154 | 30 TABLET, FILM COATED in 1 BOTTLE (68645-571-54) | 2004-10-28 | 0000-00-00 | No | No | Current |