Home > National Drug Code (NDC) > ACETAMINOPHEN

ACETAMINOPHEN - 51645-601-10 - (ACETAMINOPHEN)

Alphabetical Index


Drug Information of ACETAMINOPHEN

Product NDC: 51645-601
Proprietary Name: ACETAMINOPHEN
Non Proprietary Name: ACETAMINOPHEN
Active Ingredient(s): 500    mg/1 & nbsp;   ACETAMINOPHEN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ACETAMINOPHEN

Product NDC: 51645-601
Labeler Name: Gemini Pharmaceuticals, Inc. dba ONDRA Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120330

Package Information of ACETAMINOPHEN

Package NDC: 51645-601-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (51645-601-10)

NDC Information of ACETAMINOPHEN

NDC Code 51645-601-10
Proprietary Name ACETAMINOPHEN
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (51645-601-10)
Product NDC 51645-601
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACETAMINOPHEN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120330
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Gemini Pharmaceuticals, Inc. dba ONDRA Pharmaceuticals
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ACETAMINOPHEN


General Information