Sertraline Hydrochloride
- Product NDC
- 50436-0834
- 11-digit product format
- 504360834
- Labeler code
- 50436
- Product ID
- 50436-0834_23ffc307-bb39-4d45-a331-3b532ef8142b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sertraline Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA077397
- Marketing category
- ANDA
- Marketing start
- 2016-07-21
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-0834-1 | Sertraline Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
| 50436-0834-3 | Sertraline Hydrochloride | 90 in 1 BOTTLE | TABLET | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0834 | SERTRALINE HYDROCHLORIDE TABLET [UNIT DOSE SERVICES] | 4 | Legacy NDC, 2 package rows | 20190307_2ff82f14-5035-4716-9372-ebc496cd34ec.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0834-1 | 50436083401 | 30 in 1 BOTTLE | Historical |
| 50436-0834-3 | 50436083403 | 90 in 1 BOTTLE | Historical |