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Rx Act Nasal Decongestant - 37808-432-62 - (Pseudoephedrine HCl)

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Drug Information of Rx Act Nasal Decongestant

Product NDC: 37808-432
Proprietary Name: Rx Act Nasal Decongestant
Non Proprietary Name: Pseudoephedrine HCl
Active Ingredient(s): 30    mg/1 & nbsp;   Pseudoephedrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Rx Act Nasal Decongestant

Product NDC: 37808-432
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060213

Package Information of Rx Act Nasal Decongestant

Package NDC: 37808-432-62
Package Description: 1 BLISTER PACK in 1 CARTON (37808-432-62) > 24 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Rx Act Nasal Decongestant

NDC Code 37808-432-62
Proprietary Name Rx Act Nasal Decongestant
Package Description 1 BLISTER PACK in 1 CARTON (37808-432-62) > 24 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 37808-432
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Pseudoephedrine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060213
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H E B
Substance Name PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Rx Act Nasal Decongestant


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