Class II · Moderate risk
Naproxen Sodum Tablets USP 220 mg
CGMP Deviations
National Drug Code
Is NDC 62207-0762-36 recalled?
Naproxen Sodium · 50000 TABLET, FILM COATED in 1 POUCH (62207-762-36)
Yes — this exact package was recalled
1 FDA recall names the code 62207-0762-36 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Naproxen Sodium
- Strength
- NAPROXEN SODIUM 220 mg/1
- Form
- Tablet, Film Coated
- Labeler
- Granules India Limited
- Type
- Drug for Further Processing
- Product code
- 62207-0762
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 62207-0773 Ranitidine 1
Free recall alerts
Know the day your medication is recalled
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