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Loperamide Hydrochloride - 37808-645-26 - (loperamide HCl)

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Drug Information of Loperamide Hydrochloride

Product NDC: 37808-645
Proprietary Name: Loperamide Hydrochloride
Non Proprietary Name: loperamide HCl
Active Ingredient(s): 1    mg/7.5mL & nbsp;   loperamide HCl
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Loperamide Hydrochloride

Product NDC: 37808-645
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA091292
Marketing Category: ANDA
Start Marketing Date: 20120305

Package Information of Loperamide Hydrochloride

Package NDC: 37808-645-26
Package Description: 120 mL in 1 BOTTLE (37808-645-26)

NDC Information of Loperamide Hydrochloride

NDC Code 37808-645-26
Proprietary Name Loperamide Hydrochloride
Package Description 120 mL in 1 BOTTLE (37808-645-26)
Product NDC 37808-645
Product Type Name HUMAN OTC DRUG
Non Proprietary Name loperamide HCl
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20120305
Marketing Category Name ANDA
Labeler Name H E B
Substance Name LOPERAMIDE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/7.5mL
Pharmaceutical Classes

Complete Information of Loperamide Hydrochloride


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