Doxepin Hydrochloride
- Product NDC
- 0378-4811
- 11-digit product format
- 003784811
- Labeler code
- 0378
- Product ID
- 0378-4811_cdca2aa8-76d9-4d8d-b163-b08da2c482c5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- NDA022036
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-01-02
- Marketing end
- 2024-04-30
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 6 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0378-4811-93 | 00378481193 | 30 TABLET in 1 BOTTLE, PLASTIC (0378-4811-93) | 30 tablet | 2020-01-02 | 2024-04-30 | No | No | Current |