Doxepin Hydrochloride
- Product NDC
- 0527-4065
- 11-digit product format
- 005274065
- Labeler code
- 0527
- Product ID
- 0527-4065_deea4759-8189-4dd3-8d07-99b569e2206b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA212997
- Marketing category
- ANDA
- Marketing start
- 2020-07-24
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 75 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0527-4065-37 | 00527406537 | 100 CAPSULE in 1 BOTTLE (0527-4065-37) | 100 capsule | 2020-07-24 | 0000-00-00 | No | No | Current |
| 0527-4065-43 | 00527406543 | 1000 CAPSULE in 1 BOTTLE (0527-4065-43) | 1000 capsule | 2020-07-24 | 0000-00-00 | No | No | Current |