SERTRALINE HYDROCHLORIDE
- Product NDC
- 68071-3309
- 11-digit product format
- 680713309
- Labeler code
- 68071
- Product ID
- 68071-3309_bb2b3c0a-6724-4030-e053-2a95a90ac206
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SERTRALINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA202825
- Marketing category
- ANDA
- Marketing start
- 2017-02-09
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3309-2 | 68071330902 | 20 TABLET, FILM COATED in 1 BOTTLE (68071-3309-2) | 2017-06-08 | 0000-00-00 | No | No | Current |
| 68071-3309-3 | 68071330903 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3309-3) | 2017-06-08 | 0000-00-00 | No | No | Current |
| 68071-3309-5 | 68071330905 | 56 TABLET, FILM COATED in 1 BOTTLE (68071-3309-5) | 2017-06-08 | 0000-00-00 | No | No | Current |
| 68071-3309-6 | 68071330906 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-3309-6) | 2017-06-08 | 0000-00-00 | No | No | Current |
| 68071-3309-8 | 68071330908 | 28 TABLET, FILM COATED in 1 BOTTLE (68071-3309-8) | 2017-06-08 | 0000-00-00 | No | No | Current |
| 68071-3309-9 | 68071330909 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3309-9) | 2017-06-08 | 0000-00-00 | No | No | Current |