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Nasal Decongestant

NDC 70677-1017 · Strategic Sourcing Services LLC

Generic namePseudoephedrine HCl
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)PSEUDOEPHEDRINE HYDROCHLORIDE
Strength30 mg/1
Pharmacologic classAdrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

70677-1017-1 — 1 BLISTER PACK in 1 CARTON (70677-1017-1) / 24 TABLET, FILM COATED in 1 BLISTER PACK

70677-1017-2 — 2 BLISTER PACK in 1 CARTON (70677-1017-2) / 24 TABLET, FILM COATED in 1 BLISTER PACK

70677-1017-3 — 4 BLISTER PACK in 1 CARTON (70677-1017-3) / 24 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70000-0656 — Pseudoephedrine hydrochloride, 70000-0677 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 70000-0719 — guaifenesin, pseudoephedrine hydrochloride, 70000-0720 — guaifenesin and pseudoephedrine hydrochloride, 70000-0735 — Pseudoephedrine HCl, 70000-0772 — fexofenadine hydrochloride, pseudoephedrine hydrochloride, 70518-4526 — Brompheniramine Maleate, Pseudoephedrine Hydrochloride and Dextromethorphan Hydrobromide, 70677-0001 — Pseudoephedrine Hydrochloride, 70677-1010 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 70677-1011 — Guaifenesin and Pseudoephedrine HCL, 70677-1019 — Pseudoephedrine hydrochloride, 70677-1020 — Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride, 70677-1263 — Guaifenesin and Pseudoephedrine HCl, 70677-1272 — guaifenesin and pseudoephedrine hydrochloride, 70677-1273 — guaifenesin, pseudoephedrine hydrochloride, 70677-1311 — Cetirizine hydrochloride, Pseudoephedrine hydrochloride, 70677-1315 — fexofenadine hydrochloride, pseudoephedrine hydrochloride, 71179-816 — Naproxen Sodium and Pseudoephedrine Hydrochloride, 71205-197 — Pseudoephedrine HCl, 71930-026 — Brompheniramine maleate, pseudoephedrine hydrochloride,, +279 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels