Naproxen - 49999-049-28 - (Naproxen)

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Drug Information of Naproxen

Product NDC: 49999-049
Proprietary Name: Naproxen
Non Proprietary Name: Naproxen
Active Ingredient(s): 375    mg/1 & nbsp;   Naproxen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen

Product NDC: 49999-049
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078250
Marketing Category: ANDA
Start Marketing Date: 20111104

Package Information of Naproxen

Package NDC: 49999-049-28
Package Description: 28 TABLET in 1 BOTTLE, PLASTIC (49999-049-28)

NDC Information of Naproxen

NDC Code 49999-049-28
Proprietary Name Naproxen
Package Description 28 TABLET in 1 BOTTLE, PLASTIC (49999-049-28)
Product NDC 49999-049
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111104
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name NAPROXEN
Strength Number 375
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Naproxen


General Information