Doxepin Hydrochloride
- Product NDC
- 68788-7731
- 11-digit product format
- 687887731
- Labeler code
- 68788
- Product ID
- 68788-7731_7abc750e-d135-4c75-8d21-06b4b2a0afbe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA211603
- Marketing category
- ANDA
- Marketing start
- 2020-07-01
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68788-7731-3 | 68788773103 | 30 CAPSULE in 1 BOTTLE (68788-7731-3) | 30 capsule | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7731-6 | 68788773106 | 60 CAPSULE in 1 BOTTLE (68788-7731-6) | 60 capsule | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7731-9 | 68788773109 | 90 CAPSULE in 1 BOTTLE (68788-7731-9) | 90 capsule | 2020-07-01 | 0000-00-00 | No | No | Current |