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Latanoprost - 21695-986-25 - (Latanoprost)

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Drug Information of Latanoprost

Product NDC: 21695-986
Proprietary Name: Latanoprost
Non Proprietary Name: Latanoprost
Active Ingredient(s): 50    ug/mL & nbsp;   Latanoprost
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Latanoprost

Product NDC: 21695-986
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201006
Marketing Category: ANDA
Start Marketing Date: 20110322

Package Information of Latanoprost

Package NDC: 21695-986-25
Package Description: 1 BOTTLE in 1 CARTON (21695-986-25) > 2.5 mL in 1 BOTTLE

NDC Information of Latanoprost

NDC Code 21695-986-25
Proprietary Name Latanoprost
Package Description 1 BOTTLE in 1 CARTON (21695-986-25) > 2.5 mL in 1 BOTTLE
Product NDC 21695-986
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Latanoprost
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20110322
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name LATANOPROST
Strength Number 50
Strength Unit ug/mL
Pharmaceutical Classes Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient]

Complete Information of Latanoprost


General Information