Sertraline Hydrochloride
- Product NDC
- 55700-340
- 11-digit product format
- 557000340
- Labeler code
- 55700
- Product ID
- 55700-340_22f80842-a3dd-47f8-8151-693880ee39b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sertraline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077206
- Marketing category
- ANDA
- Marketing start
- 2007-02-06
- Marketing end
- 0000-00-00
- Substance
- SERTRALINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 55700-340-30 | 55700034030 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-340-30) | 2015-12-07 | 0000-00-00 | No | No | Current |
| 55700-340-60 | 55700034060 | 60 TABLET, FILM COATED in 1 BOTTLE (55700-340-60) | 2015-12-07 | 0000-00-00 | No | No | Current |
| 55700-340-90 | 55700034090 | 90 TABLET, FILM COATED in 1 BOTTLE (55700-340-90) | 2015-12-07 | 0000-00-00 | No | No | Current |