Zoloft
- Product NDC
- 67544-080
- 11-digit product format
- 675440080
- Labeler code
- 67544
- Product ID
- 67544-080_bedd246d-d8fe-4d00-98bd-8042d81f964b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SERTRALINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- NDA019839
- Marketing category
- NDA
- Marketing start
- 1992-02-11
- Marketing end
- 0000-00-00
- Substance
- SERTRALINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 67544-080-15 | EA - Each | 67544-080 | 65d425a1-3560-42cd-84fc-9cdde63c7051 | 1 | 2013-08-02 |
| 67544-080-30 | EA - Each | 67544-080 | ba1b7176-892c-40c5-b1ba-83b3db59c22f | 1 | 2013-08-02 |
| 67544-080-45 | EA - Each | 67544-080 | ba0efdd3-a2db-4a3e-8ad9-75fda2e0b493 | 1 | 2013-08-02 |
| 67544-080-53 | EA - Each | 67544-080 | 276d361e-fe5d-4bed-9486-f46bafcbc732 | 1 | 2013-08-02 |
| 67544-080-60 | EA - Each | 67544-080 | 07a7229a-3230-492c-8a22-a985c186eb9e | 1 | 2013-08-02 |
| 67544-080-71 | EA - Each | 67544-080 | 2426e713-25fa-4061-909e-63e0ea171667 | 1 | 2013-08-02 |
| 67544-080-73 | EA - Each | 67544-080 | eb71239c-3cac-464b-ba7a-744186ff08b1 | 1 | 2014-04-03 |
| 67544-080-74 | EA - Each | 67544-080 | 962df3b4-836b-4c89-b1f3-2cd3c1e48e60 | 1 | 2014-04-03 |
| 67544-080-80 | EA - Each | 67544-080 | 5f034e02-3836-488b-90a8-a7d672e0295b | 1 | 2013-08-02 |