Details for New Drug Application (NDA): 212517
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The generic ingredient in NAPROXEN is naproxen sodium; pseudoephedrine hydrochloride. There are forty-two drug master file entries for this compound. Nine suppliers are listed for this compound. Additional details are available on the naproxen sodium; pseudoephedrine hydrochloride profile page.
Summary for 212517
| Tradename: | NAPROXEN |
| Applicant: | Sciegen Pharms Inc |
| Ingredient: | naproxen |
| Patents: | 0 |
Pharmacology for NDA: 212517
| Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 212517
Suppliers and Packaging for NDA: 212517
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| NAPROXEN | naproxen | TABLET;ORAL | 212517 | ANDA | Medsource Pharmaceuticals | 45865-238 | 45865-238-60 | 60 TABLET in 1 BOTTLE (45865-238-60) |
| NAPROXEN | naproxen | TABLET;ORAL | 212517 | ANDA | A-S Medication Solutions | 50090-5645 | 50090-5645-0 | 15 TABLET in 1 BOTTLE (50090-5645-0) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 250MG | ||||
| Approval Date: | Feb 21, 2020 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 375MG | ||||
| Approval Date: | Feb 21, 2020 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 500MG | ||||
| Approval Date: | Feb 21, 2020 | TE: | AB | RLD: | No | ||||
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