paroxetine
- Product NDC
- 53808-0750
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PAROXETINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA075356
- Marketing category
- ANDA
- Substance
- PAROXETINE HYDROCHLORIDE
- Current FDA listing
- Historical FDA.report record
Related Records
Packages
No records found.
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| PAROXETINE TABLETS USP 10 mg, 20 mg, 30 mg and 40 mg | State of Florida DOH Central Pharmacy | 2010-05-29 | HUMAN PRESCRIPTION DRUG LABEL | 1 |