Details for New Drug Application (NDA): 202807
✉ Email this page to a colleague
The generic ingredient in NAPROXEN SODIUM is naproxen sodium; pseudoephedrine hydrochloride. There are forty-two drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the naproxen sodium; pseudoephedrine hydrochloride profile page.
Summary for 202807
Tradename: | NAPROXEN SODIUM |
Applicant: | Catalent |
Ingredient: | naproxen sodium |
Patents: | 0 |
Pharmacology for NDA: 202807
Mechanism of Action | Cyclooxygenase Inhibitors |
Suppliers and Packaging for NDA: 202807
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
NAPROXEN SODIUM | naproxen sodium | CAPSULE;ORAL | 202807 | ANDA | Walgreens | 0363-7510 | 0363-7510-20 | 1 BOTTLE, PLASTIC in 1 BOX (0363-7510-20) / 20 TABLET in 1 BOTTLE, PLASTIC |
NAPROXEN SODIUM | naproxen sodium | CAPSULE;ORAL | 202807 | ANDA | Walgreens | 0363-7510 | 0363-7510-40 | 1 BOTTLE, PLASTIC in 1 BOX (0363-7510-40) / 40 TABLET in 1 BOTTLE, PLASTIC |
Profile for product number 001
Active Rx/OTC/Discontinued: | OTC | Dosage: | CAPSULE;ORAL | Strength | EQ 200MG BASE | ||||
Approval Date: | Jan 4, 2019 | TE: | RLD: | No |
Complete Access Available with Subscription