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Diclofenac Sodium - 21695-710-25 - (Diclofenac Sodium)

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Drug Information of Diclofenac Sodium

Product NDC: 21695-710
Proprietary Name: Diclofenac Sodium
Non Proprietary Name: Diclofenac Sodium
Active Ingredient(s): 1    mg/mL & nbsp;   Diclofenac Sodium
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Diclofenac Sodium

Product NDC: 21695-710
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078792
Marketing Category: ANDA
Start Marketing Date: 20071228

Package Information of Diclofenac Sodium

Package NDC: 21695-710-25
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (21695-710-25) > 2.5 mL in 1 BOTTLE, DROPPER

NDC Information of Diclofenac Sodium

NDC Code 21695-710-25
Proprietary Name Diclofenac Sodium
Package Description 1 BOTTLE, DROPPER in 1 CARTON (21695-710-25) > 2.5 mL in 1 BOTTLE, DROPPER
Product NDC 21695-710
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diclofenac Sodium
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20071228
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name DICLOFENAC SODIUM
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Diclofenac Sodium


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