Etodolac - 21695-049-60 - (Etodolac)

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Drug Information of Etodolac

Product NDC: 21695-049
Proprietary Name: Etodolac
Non Proprietary Name: Etodolac
Active Ingredient(s): 300    mg/1 & nbsp;   Etodolac
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Etodolac

Product NDC: 21695-049
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075126
Marketing Category: ANDA
Start Marketing Date: 19990916

Package Information of Etodolac

Package NDC: 21695-049-60
Package Description: 60 CAPSULE, GELATIN COATED in 1 BOTTLE (21695-049-60)

NDC Information of Etodolac

NDC Code 21695-049-60
Proprietary Name Etodolac
Package Description 60 CAPSULE, GELATIN COATED in 1 BOTTLE (21695-049-60)
Product NDC 21695-049
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 19990916
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name ETODOLAC
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Etodolac


General Information