Doxepin Hydrochloride
- Product NDC
- 0904-6973
- 11-digit product format
- 009046973
- Labeler code
- 0904
- Product ID
- 0904-6973_41d8f133-97e0-4e9f-ae57-3ef063e24121
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA071422
- Marketing category
- ANDA
- Marketing start
- 2017-09-01
- Marketing end
- 2022-02-28
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 100 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 |
|---|
| 0904-6973-61 | 00904697361 | 100 BLISTER PACK in 1 CARTON (0904-6973-61) > 1 CAPSULE in 1 BLISTER PACK | 100 blister pack | 2017-09-01 | 2022-02-28 | No | No | Current |