# NAPROXEN SODIUM
> **ANDA204872** · Abbreviated New Drug Application (Generic) · Sponsor: LNK INTL INC · Approved 2017-01-23
## Drug
- **FDA Application Number:** ANDA204872
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** NAPROXEN SODIUM
- **Generic name:** NAPROXEN SODIUM
- **Active ingredients:** NAPROXEN SODIUM
- **Dosage form:** TABLET
- **Route:** ORAL
- **Marketing status:** Over-the-counter
- **Sponsor:** LNK INTL INC
- **Manufacturer:** Amerisource Bergen
- **First approval:** 2017-01-23
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=204872)
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