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PIRMELLA 7/7/7 - 68180-892-13 - (NORETHINDRONE AND ETHINYL ESTRADIOL)

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Drug Information of PIRMELLA 7/7/7

Product NDC: 68180-892
Proprietary Name: PIRMELLA 7/7/7
Non Proprietary Name: NORETHINDRONE AND ETHINYL ESTRADIOL
Active Ingredient(s):    & nbsp;   NORETHINDRONE AND ETHINYL ESTRADIOL
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of PIRMELLA 7/7/7

Product NDC: 68180-892
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201510
Marketing Category: ANDA
Start Marketing Date: 20130515

Package Information of PIRMELLA 7/7/7

Package NDC: 68180-892-13
Package Description: 3 BLISTER PACK in 1 CARTON (68180-892-13) > 1 KIT in 1 BLISTER PACK (68180-892-11)

NDC Information of PIRMELLA 7/7/7

NDC Code 68180-892-13
Proprietary Name PIRMELLA 7/7/7
Package Description 3 BLISTER PACK in 1 CARTON (68180-892-13) > 1 KIT in 1 BLISTER PACK (68180-892-11)
Product NDC 68180-892
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NORETHINDRONE AND ETHINYL ESTRADIOL
Dosage Form Name KIT
Route Name
Start Marketing Date 20130515
Marketing Category Name ANDA
Labeler Name Lupin Pharmaceuticals, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of PIRMELLA 7/7/7


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