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Anagrelide Hydrochloride - 0378-6869-05 - (anagrelide hydrochloride)

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Drug Information of Anagrelide Hydrochloride

Product NDC: 0378-6869
Proprietary Name: Anagrelide Hydrochloride
Non Proprietary Name: anagrelide hydrochloride
Active Ingredient(s): 1    mg/1 & nbsp;   anagrelide hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Anagrelide Hydrochloride

Product NDC: 0378-6869
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076811
Marketing Category: ANDA
Start Marketing Date: 20110228

Package Information of Anagrelide Hydrochloride

Package NDC: 0378-6869-05
Package Description: 500 CAPSULE in 1 BOTTLE, PLASTIC (0378-6869-05)

NDC Information of Anagrelide Hydrochloride

NDC Code 0378-6869-05
Proprietary Name Anagrelide Hydrochloride
Package Description 500 CAPSULE in 1 BOTTLE, PLASTIC (0378-6869-05)
Product NDC 0378-6869
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name anagrelide hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110228
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name ANAGRELIDE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Decreased Platelet Production [PE],Platelet-reducing Agent [EPC],Phosphodiesterase 3 Inhibitors [MoA]

Complete Information of Anagrelide Hydrochloride


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