Doxepin Hydrochloride
- Product NDC
- 55700-831
- 11-digit product format
- 557000831
- Labeler code
- 55700
- Product ID
- 55700-831_8c9e0769-9b93-4526-b6fb-55c5cd34f4de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA211603
- Marketing category
- ANDA
- Marketing start
- 2019-12-23
- 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
- 2021-12-31
- 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 |
|---|
| 55700-831-30 | 55700083130 | 30 CAPSULE in 1 BOTTLE (55700-831-30) | 30 capsule | 2019-12-23 | 0000-00-00 | No | No | Current |