Doxepin Hydrochloride
- Product NDC
- 72162-2228
- 11-digit product format
- 721622228
- Labeler code
- 72162
- Product ID
- 72162-2228_aed9708c-54a5-4b76-b137-4cfcb47e89c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA213474
- Marketing category
- ANDA
- Marketing start
- 2021-05-01
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 75 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 |
|---|
| 72162-2228-1 | 72162222801 | 100 CAPSULE in 1 BOTTLE (72162-2228-1) | 100 capsule | 2024-01-26 | No | No | Historical |