Doxepin Hydrochloride
- Product NDC
- 70518-1380
- 11-digit product format
- 705181380
- Labeler code
- 70518
- Product ID
- 70518-1380_92a34ee8-25a8-09e6-e053-2995a90a4eb5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207482
- Marketing category
- ANDA
- Marketing start
- 2018-08-20
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record