Doxepin Hydrochloride
- Product NDC
- 35356-424
- 11-digit product format
- 353560424
- Labeler code
- 35356
- Product ID
- 35356-424_eeab8714-5d71-48d1-88d9-4d809786808b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxepin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA070791
- Marketing category
- ANDA
- Marketing start
- 1986-05-13
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record