Naproxen Sodium And Diphenhydramine Hcl 62207-0814
Product NDC
62207-0814- Manufacturer
- Granules India Ltd
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- February 20, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA213663
Active Ingredients
| Ingredient | Strength |
|---|---|
| Diphenhydramine Hydrochloride | 25 mg/1 |
| Naproxen Sodium | 220 mg/1 |
Drug Class
Anti-Inflammatory AgentsNon-Steroidal [CS]Cyclooxygenase Inhibitors [MoA]
Packaging Options(4)
37500 TABLET, FILM COATED in 1 POUCH (62207-814-38)
7500 TABLET, FILM COATED in 1 POUCH (62207-814-39)
500 TABLET, FILM COATED in 1 BOTTLE (62207-814-47)
1 BOTTLE in 1 CARTON (62207-814-95) / 20 TABLET, FILM COATED in 1 BOTTLE