Details for New Drug Application (NDA): 074140
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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. Ten suppliers are listed for this compound. Additional details are available on the naproxen sodium; pseudoephedrine hydrochloride profile page.
Pharmacology for NDA: 074140
Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 074140
Suppliers and Packaging for NDA: 074140
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
NAPROXEN | naproxen | TABLET;ORAL | 074140 | ANDA | Northwind Pharmaceuticals, LLC | 51655-457 | 51655-457-20 | 20 TABLET in 1 BOTTLE, PLASTIC (51655-457-20) |
NAPROXEN | naproxen | TABLET;ORAL | 074140 | ANDA | Northwind Pharmaceuticals, LLC | 51655-457 | 51655-457-25 | 60 TABLET in 1 BOTTLE, PLASTIC (51655-457-25) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 250MG | ||||
Approval Date: | Dec 21, 1993 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 375MG | ||||
Approval Date: | Dec 21, 1993 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 500MG | ||||
Approval Date: | Dec 21, 1993 | TE: | AB | RLD: | No |
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