Sertraline Hydrochloride
- Product NDC
- 63629-8128
- 11-digit product format
- 636298128
- Labeler code
- 63629
- Product ID
- 63629-8128_0710f6fa-137e-4521-8759-29b272217824
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sertraline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 63629-8128-1 | 63629812801 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-8128-1) | 2019-07-25 | 0000-00-00 | No | No | Current |
| 63629-8128-2 | 63629812802 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-8128-2) | 2019-07-25 | 0000-00-00 | No | No | Current |