Doxepin Hydrochloride
- Product NDC
- 45865-849
- 11-digit product format
- 458650849
- Labeler code
- 45865
- Product ID
- 45865-849_7e04402f-279b-6a96-e053-2991aa0aa4ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxepin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Medsource Pharmaceuticals
- Application
- ANDA070791
- Marketing category
- ANDA
- Marketing start
- 1986-05-13
- Marketing end
- 2019-09-30
- 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