Doxepin Hydrochloride
- Product NDC
- 71335-0780
- 11-digit product format
- 713350780
- Labeler code
- 71335
- Product ID
- 71335-0780_5ff16ea4-9866-4d88-9f17-9687c8d5b66b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207482
- Marketing category
- ANDA
- Marketing start
- 2017-06-28
- 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 |
|---|
| 71335-0780-1 | 71335078001 | 30 CAPSULE in 1 BOTTLE (71335-0780-1) | 30 capsule | 2018-04-19 | 0000-00-00 | No | No | Current |
| 71335-0780-2 | 71335078002 | 60 CAPSULE in 1 BOTTLE (71335-0780-2) | 60 capsule | 2018-04-19 | 0000-00-00 | No | No | Current |
| 71335-0780-3 | 71335078003 | 28 CAPSULE in 1 BOTTLE (71335-0780-3) | 28 capsule | 2018-04-19 | 0000-00-00 | No | No | Current |
| 71335-0780-4 | 71335078004 | 18 CAPSULE in 1 BOTTLE (71335-0780-4) | 18 capsule | 2018-04-19 | 0000-00-00 | No | No | Current |
| 71335-0780-5 | 71335078005 | 90 CAPSULE in 1 BOTTLE (71335-0780-5) | 90 capsule | 2018-04-19 | 0000-00-00 | No | No | Current |