SEARCH RESULTS for: pseudoephedrine hydrochloride (414 results)

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CETIRIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE (cetirizine hcl, pseudoephedrine hcl) tablet, extended release

NDC Code(s): 50090-1098-0, 50090-1098-1
• Packager: A-S Medication Solutions
• This is a repackaged label.
• Source NDC Code(s): 45802-721

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CETIRIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE (cetirizine hcl, pseudoephedrine hcl) tablet, extended release

NDC Code(s): 68258-8907-2
• Packager: Dispensing Solutions, Inc.
• This is a repackaged label.
• Source NDC Code(s): 45802-721

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CETIRIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE (cetirizine hcl, pseudoephedrine hcl) tablet, extended release

NDC Code(s): 63187-955-12, 63187-955-24
• Packager: Proficient Rx LP
• This is a repackaged label.
• Source NDC Code(s): 45802-721

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FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE tablet, film coated, extended release

NDC Code(s): 54868-6087-0, 54868-6087-1, 54868-6087-2
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0093-1130

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FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE tablet, film coated, extended release

NDC Code(s): 21695-820-14
• Packager: Rebel Distributors Corp
• This is a repackaged label.
• Source NDC Code(s): 0955-1705

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GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE EXTENDED RELEASE (guaifenesin, pseudoephedrine hydrochloride) tablet, extended release

NDC Code(s): 63187-960-18
• Packager: Proficient Rx LP
• This is a repackaged label.
• Source NDC Code(s): 45802-230

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MUCINEX D (guaifenesin and pseudoephedrine hydrochloride) tablet, extended release

NDC Code(s): 68258-3035-1
• Packager: Dispensing Solutions Inc.
• This is a repackaged label.
• Source NDC Code(s): 63824-057-18

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MUCINEX D (guaifenesin and pseudoephedrine hydrochloride) tablet, extended release

NDC Code(s): 54868-5849-0
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 63824-057

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PSEUDOEPHEDRINE HYDROCHLORIDE (pseudoephedrine hcl) tablet, film coated

NDC Code(s): 50090-5615-0, 50090-5615-1
• Packager: A-S Medication Solutions
• This is a repackaged label.
• Source NDC Code(s): 45802-432

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PSEUDOEPHEDRINE HYDROCHLORIDE (pseudoephedrine hcl) tablet, film coated

NDC Code(s): 71205-197-24
• Packager: Proficient Rx LP
• This is a repackaged label.
• Source NDC Code(s): 45802-432

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PSEUDOEPHEDRINE HYDROCHLORIDE tablet

NDC Code(s): 50090-4546-0, 50090-4546-1, 50090-4546-3, 50090-4546-4, view more
50090-4546-5
• Packager: A-S Medication Solutions
• This is a repackaged label.
• Source NDC Code(s): 0904-6728

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PSEUDOEPHEDRINE HYDROCHLORIDE tablet, film coated

NDC Code(s): 50090-5554-0
• Packager: A-S Medication Solutions
• This is a repackaged label.
• Source NDC Code(s): 51660-204

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PSEUDOEPHEDRINE HYDROCHLORIDE tablet, film coated

NDC Code(s): 54868-1973-1, 54868-1973-3, 54868-1973-4
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0904-5125

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12 HOUR ALLERGY D (cetirizine hydrochloride, pseudoephedrine hydrochloride) tablet, film coated, extended release

NDC Code(s): 41250-728-53, 41250-728-62
• Packager: Meijer Distribution Inc

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12 HOUR NASAL DECONGESTANT (pseudoephedrine hydrochloride) tablet, film coated

NDC Code(s): 70000-0656-1
• Packager: CARDINAL HEALTH

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12 HOUR NASAL DECONGESTANT (pseudoephedrine hydrochloride) tablet, film coated, extended release

NDC Code(s): 59779-703-52, 59779-703-60
• Packager: CVS Pharmacy

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12HR ALLERGY AND CONGESTION RELIEF (fexofenadine hydrochloride and pseudoephedrine hydrochloride) tablet, extended release

NDC Code(s): 70000-0634-1, 70000-0634-2
• Packager: LEADER/ Cardinal Health 110, Inc.

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ABATUSS DMX (dexchlorpheniramine maleate, dextromethorphan hydrobromide, pseudoephedrine hydrochloride) liquid

NDC Code(s): 52083-625-16
• Packager: Kramer Novis

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ACTICON (dexbrompheniramine maleate, pseudoephedrine hydrochloride) liquid

NDC Code(s): 63102-105-16
• Packager: ACTIPHARMA, INC.

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ACTICON (dexbrompheniramine maleate, pseudoephedrine hydrochloride) solution

NDC Code(s): 63102-108-16
• Packager: ACTIPHARMA, INC