Doxepin Hydrochloride
- Product NDC
- 63629-7852
- 11-digit product format
- 636297852
- Labeler code
- 63629
- Product ID
- 63629-7852_005f0da3-20f2-40ae-9907-d05ff47b2ce5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxepin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071422
- Marketing category
- ANDA
- Marketing start
- 2017-09-01
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#