Doxepin Hydrochloride
- Product NDC
- 42799-935
- 11-digit product format
- 427990935
- Labeler code
- 42799
- Product ID
- 42799-935_ce3c96ec-c8e5-4241-a32c-cdc3e67f3001
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Edenbridge Pharmaceuticals LLC.
- Application
- ANDA213796
- Marketing category
- ANDA
- Marketing start
- 2022-05-02
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 150 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 |
|---|
| 42799-935-01 | 42799093501 | 100 CAPSULE in 1 BOTTLE (42799-935-01) | 100 capsule | 2022-05-02 | 0000-00-00 | No | No | Current |
| 42799-935-02 | 42799093502 | 500 CAPSULE in 1 BOTTLE (42799-935-02) | 500 capsule | 2022-05-02 | 0000-00-00 | No | No | Current |
| 42799-935-50 | 42799093550 | 50 CAPSULE in 1 BOTTLE (42799-935-50) | 50 capsule | 2022-05-02 | 0000-00-00 | No | No | Current |