SERTRALINE HYDROCHLORIDE
- Product NDC
- 63629-6755
- 11-digit product format
- 636296755
- Labeler code
- 63629
- Product ID
- 63629-6755_e4b7d5ee-0e80-4e8b-a1cd-86310c393f5f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sertraline hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA019839
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2006-03-20
- Marketing end
- 0000-00-00
- Substance
- SERTRALINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 63629-6755-1 | 63629675501 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-6755-1) | 2016-02-23 | 0000-00-00 | No | No | Current |
| 63629-6755-2 | 63629675502 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-6755-2) | 2016-02-23 | 0000-00-00 | No | No | Current |