Doxepin Hydrochloride
- Product NDC
- 49999-190
- 11-digit product format
- 499990190
- Labeler code
- 49999
- Product ID
- 49999-190_4dfd0c6c-478a-4405-9f99-2f27a6b35d2c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxepin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
- Application
- ANDA070791
- Marketing category
- ANDA
- Marketing start
- 2012-03-05
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record