Sertraline Hydrochloride
- Product NDC
- 63629-6370
- 11-digit product format
- 636296370
- Labeler code
- 63629
- Product ID
- 63629-6370_1f24b1ad-d8a1-4886-bbc8-07d16fb12713
- 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
- 25 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63629-6370-1 | 63629637001 | 15 TABLET, FILM COATED in 1 BOTTLE (63629-6370-1) | 2015-09-17 | 0000-00-00 | No | No | Current |