SERTRALINE HYDROCHLORIDE
- Product NDC
- 60760-737
- 11-digit product format
- 607600737
- Labeler code
- 60760
- Product ID
- 60760-737_f049247b-f016-0ae4-e053-2a95a90a31f5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SERTRALINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA202825
- Marketing category
- ANDA
- Marketing start
- 2018-08-21
- Marketing end
- 0000-00-00
- Substance
- SERTRALINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Cytochrome P450 2D6 Inhibitors [MoA], Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-737 | SERTRALINE HYDROCHLORIDE TABLET, FILM COATED [ST. MARY'S MEDICAL PARK PHARMACY] | 4 | Legacy NDC | 20221221_73f4bfe7-80b2-01d8-e053-2991aa0a9cb0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-737-30 | 60760073730 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-737-30) | 2018-08-21 | 0000-00-00 | No | No | Current |
| 60760-737-90 | 60760073790 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-737-90) | 2018-08-21 | 0000-00-00 | No | No | Current |