Doxepin HCL
- Product NDC
- 72189-533
- 11-digit product format
- 721890533
- Labeler code
- 72189
- Product ID
- 72189-533_0ead9074-3479-7c3d-e063-6394a90a9d27
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin HCL
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA212624
- Marketing category
- ANDA
- Marketing start
- 2024-01-11
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 25 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 |
|---|
| 72189-533-30 | 72189053330 | 30 CAPSULE in 1 BOTTLE (72189-533-30) | 30 capsule | 2024-01-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Doxepin HCL | Direct_Rx | 2024-01-11 | HUMAN PRESCRIPTION DRUG LABEL | 1 |