Doxepin Hydrochloride
- Product NDC
- 70518-1412
- 11-digit product format
- 705181412
- Labeler code
- 70518
- Product ID
- 70518-1412_92cadd5a-0c94-2f7b-e053-2995a90ae23c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207482
- Marketing category
- ANDA
- Marketing start
- 2018-09-12
- Marketing end
- 0000-00-00
- Substance
- DOXEPIN HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record