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Sunmark acid reducer - 49348-733-12 - (Ranitidine)

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Drug Information of Sunmark acid reducer

Product NDC: 49348-733
Proprietary Name: Sunmark acid reducer
Non Proprietary Name: Ranitidine
Active Ingredient(s): 75    mg/1 & nbsp;   Ranitidine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sunmark acid reducer

Product NDC: 49348-733
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076760
Marketing Category: ANDA
Start Marketing Date: 20090710

Package Information of Sunmark acid reducer

Package NDC: 49348-733-12
Package Description: 1 BOTTLE in 1 CARTON (49348-733-12) > 60 TABLET in 1 BOTTLE

NDC Information of Sunmark acid reducer

NDC Code 49348-733-12
Proprietary Name Sunmark acid reducer
Package Description 1 BOTTLE in 1 CARTON (49348-733-12) > 60 TABLET in 1 BOTTLE
Product NDC 49348-733
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090710
Marketing Category Name ANDA
Labeler Name McKesson
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Sunmark acid reducer


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