Doxepin
- Product NDC
- 72162-2474
- 11-digit product format
- 721622474
- Labeler code
- 72162
- Product ID
- 72162-2474_da27842d-9d36-4b4b-abbe-da72f998e300
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxepin hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202510
- Marketing category
- ANDA
- Marketing start
- 2022-09-12
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 3U9A0FE9N5 | DOXEPIN HYDROCHLORIDE | 1229-29-4 | DOXEPIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2474-3 | 72162247403 | 30 TABLET in 1 BOTTLE (72162-2474-3) | 30 tablet | 2025-05-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Doxepin | Bryant Ranch Prepack | 2025-05-01 | HUMAN PRESCRIPTION DRUG LABEL | 102 |