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Panadol

NDC 0135-0607 · Haleon US Holdings LLC

Generic nameacetaminophen and phenyleprine HCl
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE
Strength325; 5 mg/1; mg/1
Pharmacologic classAdrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

0135-0607-02 — 3 BLISTER PACK in 1 CARTON (0135-0607-02) / 8 TABLET, FILM COATED in 1 BLISTER PACK

0135-0607-03 — 50 PACKET in 1 CARTON (0135-0607-03) / 2 TABLET, FILM COATED in 1 PACKET (0135-0607-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0121-1882 — Acetaminophen, 0121-1971 — Acetaminophen, 0121-2094 — Acetaminophen, 0121-2316 — HYDROCODONE BITARTRATE and ACETAMINOPHEN, 0121-2823 — Acetaminophen, 0121-3141 — Acetaminophen, 0121-4772 — HYDROCODONE BITARTRATE and ACETAMINOPHEN, 0135-0537 — acetaminophen, 0135-0539 — acetaminophen, 0135-0578 — acetaminophen, chlorpheniramine maleate, phenylephrine hcl, 0135-0608 — acetaminophen and diphenhydramine HCl, 0135-0609 — acetaminophen, 0135-0620 — acetaminophen and caffeine, 0135-7011 — acetaminophen, 0135-7021 — acetaminophen and diphenhydramine HCl, 0135-7031 — acetaminophen and phenyleprine HCl, 0135-7033 — acetaminophen, dextromethorphan HBr, 0135-7034 — acetaminophen, chlorpheniramine maleate, dextromethorphan HBr, 0143-9150 — acetaminophen and ibuprofen injection, 0143-9386 — Acetaminophen, +4112 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.