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Low-Ogestrel - 54868-4850-0 - (Norgestrel and Ethinyl Estradiol)

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Drug Information of Low-Ogestrel

Product NDC: 54868-4850
Proprietary Name: Low-Ogestrel
Non Proprietary Name: Norgestrel and Ethinyl Estradiol
Active Ingredient(s):    & nbsp;   Norgestrel and Ethinyl Estradiol
Administration Route(s): ORAL
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Low-Ogestrel

Product NDC: 54868-4850
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075288
Marketing Category: ANDA
Start Marketing Date: 20090924

Package Information of Low-Ogestrel

Package NDC: 54868-4850-0
Package Description: 1 BLISTER PACK in 1 CARTON (54868-4850-0) > 1 KIT in 1 BLISTER PACK

NDC Information of Low-Ogestrel

NDC Code 54868-4850-0
Proprietary Name Low-Ogestrel
Package Description 1 BLISTER PACK in 1 CARTON (54868-4850-0) > 1 KIT in 1 BLISTER PACK
Product NDC 54868-4850
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norgestrel and Ethinyl Estradiol
Dosage Form Name KIT
Route Name ORAL
Start Marketing Date 20090924
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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Complete Information of Low-Ogestrel


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