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Directory/AARNA USA INC.

AARNA USA INC.

Drug manufacturer · manufacturer

Unclaimed listing
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18
Drug products
5
Therapeutic areas

About

AARNA USA INC. is listed in the FDA National Drug Code Directory with 18 marketed products, of which 2 are prescription drugs. Dosage forms include TABLET, CAPSULE, LIQUID, SUSPENSION, SOLUTION.

What AARNA USA INC. makes

16 of 18 products
Clear
Prescription · 2OTC · 16
Other · 12Immunology & Inflammation · 3Nutrition & Supplements · 1Pain & Anesthesia · 1CNS & Psychiatry · 1
tablet · 4suspension · 3liquid · 3suppository · 3capsule · 2solution · 1patch · 1syrup · 1
  • Childrens Acetaminophen Oral Liquid
    acetaminophen
    QuoteliquidoralOTC MONOGRAPH DRUG
  • Children Acetaminophen
    acetaminophen
    QuoteliquidoralOTC MONOGRAPH DRUG
  • ACETAMINOPHEN
    acetaminophen
    QuotetabletoralOTC MONOGRAPH DRUG
  • ACETAMINOPHEN
    acetaminophen
    QuotetabletoralOTC MONOGRAPH DRUG
  • ASPIRIN LOW DOSE
    aspirin low dose
    QuotetabletoralOTC MONOGRAPH DRUG
  • BISACODYL
    bisacodyl
    QuotesuppositoryrectalOTC MONOGRAPH DRUG
  • CHILDRENS ACETAMINOPHEN
    children acetaminophen cherry
    QuotesuspensionoralOTC MONOGRAPH DRUG
  • CHILDRENS ACETAMINOPHEN
    childrens acetaminophen oral
    QuotesuspensionoralOTC MONOGRAPH DRUG
  • Diphenhydramine HCl
    diphenhydramine hcl
    QuotecapsuleoralOTC MONOGRAPH DRUG
  • Diphenhydramine HCl
    diphenhydramine hcl
    QuotecapsuleoralOTC MONOGRAPH DRUG
  • DIPHENHYDRAMINE HCL 12.5 MG PER 5 ML
    diphenhydramine hcl 12.5 mg per 5 ml
    QuotesolutionoralOTC MONOGRAPH DRUG
  • Lidocaine Patch
    lidocaine 4% maximum strength 24 hr
    QuotepatchtopicalOTC MONOGRAPH DRUG
  • Magnesium Citrate
    magnesium citrate
    QuoteliquidoralOTC MONOGRAPH DRUG
  • Senna
    sennosides
    QuotesyruporalOTC MONOGRAPH DRUG
  • SENNA
    sennosides
    QuotetabletoralOTC MONOGRAPH DRUG
  • SIMETHICONE INFANT
    simethicone
    QuotesuspensionoralOTC MONOGRAPH DRUG

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Contact

Email and website are not published in the public registries — they are added when the listing is claimed.

From the FDA NDC Directory, refreshed 2026-08-16.

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