# NAPROXEN SODIUM AND PSEUDOEPHEDRINE HYDROCHLORIDE
> **ANDA077381** · Abbreviated New Drug Application (Generic) · Sponsor: DR REDDYS LABS INC · Approved 2006-09-27
## Drug
- **FDA Application Number:** ANDA077381
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** NAPROXEN SODIUM AND PSEUDOEPHEDRINE HYDROCHLORIDE
- **Generic name:** Naproxen Sodium
- **Active ingredients:** NAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE
- **Dosage form:** TABLET, EXTENDED RELEASE
- **Route:** ORAL
- **Marketing status:** Over-the-counter
- **Sponsor:** DR REDDYS LABS INC
- **First approval:** 2006-09-27
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=077381)
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