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pain relief - 37808-759-26 - (Acetaminophen)

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Drug Information of pain relief

Product NDC: 37808-759
Proprietary Name: pain relief
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 160    mg/5mL & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of pain relief

Product NDC: 37808-759
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110301

Package Information of pain relief

Package NDC: 37808-759-26
Package Description: 1 BOTTLE in 1 CARTON (37808-759-26) > 118 mL in 1 BOTTLE

NDC Information of pain relief

NDC Code 37808-759-26
Proprietary Name pain relief
Package Description 1 BOTTLE in 1 CARTON (37808-759-26) > 118 mL in 1 BOTTLE
Product NDC 37808-759
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20110301
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name H E B
Substance Name ACETAMINOPHEN
Strength Number 160
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of pain relief


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