# NORTRIPTYLINE HYDROCHLORIDE
> **ANDA074835** · Abbreviated New Drug Application (Generic) · Sponsor: AUROBINDO PHARMA LTD · Approved 1997-06-30
## Drug
- **FDA Application Number:** ANDA074835
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** NORTRIPTYLINE HYDROCHLORIDE
- **Generic name:** Nortriptyline Hydrochloride
- **Active ingredients:** NORTRIPTYLINE HYDROCHLORIDE
- **Dosage form:** CAPSULE
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** AUROBINDO PHARMA LTD
- **First approval:** 1997-06-30
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=074835)
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