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Kelnor 1/35 - 0555-9064-58 - (ethynodiol diacetate and ethinyl estradiol)

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Drug Information of Kelnor 1/35

Product NDC: 0555-9064
Proprietary Name: Kelnor 1/35
Non Proprietary Name: ethynodiol diacetate and ethinyl estradiol
Active Ingredient(s):    & nbsp;   ethynodiol diacetate and ethinyl estradiol
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Kelnor 1/35

Product NDC: 0555-9064
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076785
Marketing Category: ANDA
Start Marketing Date: 20050620

Package Information of Kelnor 1/35

Package NDC: 0555-9064-58
Package Description: 6 BLISTER PACK in 1 CARTON (0555-9064-58) > 1 KIT in 1 BLISTER PACK

NDC Information of Kelnor 1/35

NDC Code 0555-9064-58
Proprietary Name Kelnor 1/35
Package Description 6 BLISTER PACK in 1 CARTON (0555-9064-58) > 1 KIT in 1 BLISTER PACK
Product NDC 0555-9064
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ethynodiol diacetate and ethinyl estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20050620
Marketing Category Name ANDA
Labeler Name Barr Laboratories Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Kelnor 1/35


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