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Listings are compiled from public records — the NPPES national provider registry and the FDA National Drug Code Directory. Pharmacy Flow does not verify unclaimed listings and publishes no pricing for them.

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Directory/Health Pharma USA LLC

Health Pharma USA LLC

Drug manufacturer · manufacturer

Unclaimed listing
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15
Drug products
4
Therapeutic areas

About

Health Pharma USA LLC is listed in the FDA National Drug Code Directory with 15 marketed products. Dosage forms include CAPSULE, TABLET.

What Health Pharma USA LLC makes

13 of 15 products
Clear
OTC · 15
Other · 10Immunology & Inflammation · 3CNS & Psychiatry · 1Respiratory & Allergy · 1
tablet · 13capsule · 2
  • Pain Reliever
    acetaminophen
    Quotetablet, film coatedoralOTC MONOGRAPH DRUG
  • Acetaminophen
    acetaminophen
    Quotetablet, film coatedoralOTC MONOGRAPH DRUG
  • Acetaminophen 250 mg Aspirin 250 mg Caffeine 65 mg
    acetaminophen 250 mg aspirin 250 mg caffeine 65 mg
    Quotetablet, film coatedoralOTC MONOGRAPH DRUG
  • Acetaminophen 500 Pyrilamine Maleate 15 and Caffeine 60
    acetaminophen 500mg pyrilamine maleate 15mg and caffeine 60mg tablets
    Quotetablet, film coatedoralOTC MONOGRAPH DRUG
  • Aspirin
    aspirin
    Quotetablet, film coatedoralOTC MONOGRAPH DRUG
  • Nighttime Sleep Aid
    diphenhydramine hcl 25 mg
    Quotetablet, coatedoralOTC MONOGRAPH DRUG
  • Allergy Relief
    diphenhydramine hydrochloride
    QuotetabletoralOTC MONOGRAPH DRUG
  • Diphenhydramine Hydrochloride
    diphenhydramine hydrochloride
    Quotetablet, film coatedoralOTC MONOGRAPH DRUG
  • Diphenhydramine Hydrochloride
    diphenhydramine hydrochloride
    Quotetablet, film coatedoralOTC MONOGRAPH DRUG
  • Guaifenesin 200mg
    guaifenesin
    QuotetabletoralOTC MONOGRAPH DRUG
  • Guaifenesin
    guaifenesin
    QuotetabletoralOTC MONOGRAPH DRUG
  • Mucus Relief
    guaifenesin 400 mg
    QuotetabletoralOTC MONOGRAPH DRUG
  • Pain Relief - Ibuprofen 200 mg
    ibuprofen
    Quotetablet, coatedoralANDA

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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 2026-08-15.

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