Doxepin Hydrochloride
- Product NDC
- 71335-0642
- 11-digit product format
- 713350642
- Labeler code
- 71335
- Product ID
- 71335-0642_170a56e4-4367-47a8-a9ef-85fee7fa34af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071422
- Marketing category
- ANDA
- Marketing start
- 2017-09-01
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 71335-0642-1 | 71335064201 | 30 CAPSULE in 1 BOTTLE (71335-0642-1) | 30 capsule | 2017-09-01 | 0000-00-00 | No | No | Current |
| 71335-0642-2 | 71335064202 | 60 CAPSULE in 1 BOTTLE (71335-0642-2) | 60 capsule | 2017-09-01 | 0000-00-00 | No | No | Current |
| 71335-0642-3 | 71335064203 | 18 CAPSULE in 1 BOTTLE (71335-0642-3) | 18 capsule | 2017-09-01 | 0000-00-00 | No | No | Current |
| 71335-0642-4 | 71335064204 | 90 CAPSULE in 1 BOTTLE (71335-0642-4) | 90 capsule | 2017-09-01 | 0000-00-00 | No | No | Current |
| 71335-0642-5 | 71335064205 | 180 CAPSULE in 1 BOTTLE (71335-0642-5) | 180 capsule | 2017-09-01 | 0000-00-00 | No | No | Current |