Doxepin Hydrochloride
- Product NDC
- 63629-2180
- 11-digit product format
- 636292180
- Labeler code
- 63629
- Product ID
- 63629-2180_7169479f-c59c-4aa6-b885-f0aeb59dacf0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071422
- Marketing category
- ANDA
- Marketing start
- 1987-11-09
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2180-1 | 63629218001 | 50 CAPSULE in 1 BOTTLE (63629-2180-1) | 50 capsule | 1987-11-09 | 0000-00-00 | No | No | Current |