Rite Aid Corporation

Drug manufacturer · manufacturer

Unclaimed listing

307

Drug products

Therapeutic areas

About

Rite Aid Corporation is listed in the FDA National Drug Code Directory with 307 marketed products. Dosage forms include SUPPOSITORY, OINTMENT, LOZENGE, SOLUTION/ DROPS, TABLET.

What Rite Aid Corporation makes

11 of 307 products

OTC · 307

Other · 164 Immunology & Inflammation · 44 Dermatology · 40 Respiratory & Allergy · 11 Gastrointestinal · 11 Ophthalmic · 11 Pain & Anesthesia · 9 CNS & Psychiatry · 6 Anti-infective · 6 Nutrition & Supplements · 5

tablet · 123 solution · 25 liquid · 19 capsule · 17 suspension · 14 lozenge · 12 kit · 11 patch · 11 cream · 10 gum · 10

Night Time Cold and Flu Relief
acetaminophen, dextromethorphan hbr, doxylamine succinate
Quotecapsule, liquid filledoralOTC MONOGRAPH DRUG
Night Time Cold and Flu Relief
acetaminophen, dextromethorphan hbr, doxylamine succinate
Quotecapsule, liquid filledoralOTC MONOGRAPH DRUG
nighttime severe cold and flu relief
acetaminophen, dextromethorphan hbr, doxylamine succinate, phenylephrine hcl
QuotesolutionoralOTC MONOGRAPH DRUG
Severe Nighttime Cold and Flu Relief
acetaminophen, dextromethorphan hbr, doxylamine succinate, phenylephrine hcl
Quotetablet, film coatedoralOTC MONOGRAPH DRUG
severe cold and flu relief
acetaminophen, dextromethorphan hbr, doxylamine succinate, phenylephrine hcl
QuotesolutionoralOTC MONOGRAPH DRUG
Cold and Flu Relief
acetaminophen, dextromethorphan hydrobromide, doxylamine succinate
QuoteliquidoralOTC MONOGRAPH DRUG
Nighttime Cold and Flu
acetaminophen, dextromethorphan hydrobromide, doxylamine succinate
QuoteliquidoralOTC MONOGRAPH DRUG
severe cold and flu relief
acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride
QuotesolutionoralOTC MONOGRAPH DRUG
tussin nighttime cough
dextromethorphan hydrobromide, doxylamine succinate
QuotesolutionoralOTC MONOGRAPH DRUG
sleep aid
doxylamine succinate
QuotetabletoralANDA
sleep aid
doxylamine succinate
QuotetabletoralANDA

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From the FDA NDC Directory, refreshed 2026-08-15.

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