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care one pain relief - 41520-217-78 - (Acetaminophen)

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Drug Information of care one pain relief

Product NDC: 41520-217
Proprietary Name: care one pain relief
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 650    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of care one pain relief

Product NDC: 41520-217
Labeler Name: American Sales Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075077
Marketing Category: ANDA
Start Marketing Date: 20051129

Package Information of care one pain relief

Package NDC: 41520-217-78
Package Description: 1 BOTTLE in 1 CARTON (41520-217-78) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

NDC Information of care one pain relief

NDC Code 41520-217-78
Proprietary Name care one pain relief
Package Description 1 BOTTLE in 1 CARTON (41520-217-78) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC 41520-217
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20051129
Marketing Category Name ANDA
Labeler Name American Sales Company
Substance Name ACETAMINOPHEN
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of care one pain relief


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