Doxepin
- Product NDC
- 72162-2475
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxepin hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202510
- Marketing category
- ANDA
- Substance
- DOXEPIN HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72162-2475-3 | 30 TABLET in 1 BOTTLE (72162-2475-3) | 2025-05-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Doxepin | Bryant Ranch Prepack | 2025-05-02 | HUMAN PRESCRIPTION DRUG LABEL | 101 |