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Progesterone - 57520-0490-1 - (Progesterone,)

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Drug Information of Progesterone

Product NDC: 57520-0490
Proprietary Name: Progesterone
Non Proprietary Name: Progesterone,
Active Ingredient(s): 6    [hp_X]/mL & nbsp;   Progesterone,
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Progesterone

Product NDC: 57520-0490
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20101207

Package Information of Progesterone

Package NDC: 57520-0490-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0490-1)

NDC Information of Progesterone

NDC Code 57520-0490-1
Proprietary Name Progesterone
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0490-1)
Product NDC 57520-0490
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Progesterone,
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20101207
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name PROGESTERONE
Strength Number 6
Strength Unit [hp_X]/mL
Pharmaceutical Classes

Complete Information of Progesterone


General Information