FDA Application
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NDC Search Results on Active Ingredient: ibuprofen
Click on Active Ingredient to view the label.
Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
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IBUPROFEN | 0573-0170-30 | Haleon US Holdings LLC | NDA020589 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0170-32 | Haleon US Holdings LLC | NDA020589 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0171-03 | Haleon US Holdings LLC | NDA020589 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0171-30 | Haleon US Holdings LLC | NDA020589 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0171-32 | Haleon US Holdings LLC | NDA020589 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0174-30 | Haleon US Holdings LLC | NDA020589 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0175-11 | Haleon US Holdings LLC | NDA020267 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0179-20 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020944 | HUMAN OTC DRUG | NDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0573-0180-10 | Haleon US Holdings LLC | NDA019771 | HUMAN OTC DRUG | NDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0573-0180-21 | Haleon US Holdings LLC | NDA019771 | HUMAN OTC DRUG | NDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0573-0184-16 | Haleon US Holdings LLC | NDA021374 | HUMAN OTC DRUG | NDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0573-0184-32 | Haleon US Holdings LLC | NDA021374 | HUMAN OTC DRUG | NDA |
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE; CHLORPHENIRAMINE MALEATE | 0573-0188-10 | Haleon US Holdings LLC | NDA021441 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0190-01 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0190-02 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0190-03 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0190-10 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0190-20 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0190-30 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0191-20 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020812 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0191-22 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020812 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0191-50 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020812 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0191-75 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020812 | HUMAN OTC DRUG | NDA |
IBUPROFEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE | 0573-0196-01 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE | 0573-0196-02 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE | 0573-0196-10 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE | 0573-0196-20 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0199-01 | Haleon US Holdings LLC | NDA022565 | HUMAN OTC DRUG | NDA |
IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0199-03 | Haleon US Holdings LLC | NDA022565 | HUMAN OTC DRUG | NDA |
IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0199-11 | Haleon US Holdings LLC | NDA022565 | HUMAN OTC DRUG | NDA |
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