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PhenylephrineHydrochloride,CHLORPHENIRAMINEMALEATE

PhenylephrineHydrochloride,CHLORPHENIRAMINEMALEATE · PHENYLEPHRINE HYDROCHLORIDE 10 mg/1; CHLORPHENIRAMINE MALEATE 3.5 mg/1 · Tablet · Ameripharma Labs Limited Liability Company

NDC 79706-0003-01 · 52631 TABLET in 1 PAIL · DRUG FOR FURTHER PROCESSING · View full market →

Bulk ingredient — not a finished product

This NDC is a raw material (drug for further processing) sold to drug manufacturers or compounders, not a product pharmacies dispense. Retail pricing, TE codes, fragility scores, and shortage reports don't apply to bulk listings — those attach to finished products made from this ingredient.

Medicare Part D

This is a bulk ingredient, not a dispensable product — it is a raw material sold to manufacturers and compounders, so no plan prices it.

How Part D pricing works →

NADAC price per unit

No NADAC pricing on file for this NDC — NADAC covers drugs dispensed by retail community pharmacies.

Supply fragility

Not scored — fragility is computed for NADAC-priced NDCs.

Regulatory

Application
TE code
Approval date
Patents / exclusivity

Shortage history

No FDA shortage reports for this drug or its presentations.

Recalls (this NDC)

No enforcement reports list this package NDC.

Manufacturers of PhenylephrineHydrochloride,CHLORPHENIRAMINEMALEATE (Tablet)

LabelerStrengthFirst seenLast seen
Ameripharma Labs Limited Liability CompanyPHENYLEPHRINE HYDROCHLORIDE 10 mg/1; CHLORPHENIRAMINE MALEATE 3.5 mg/1Aug 20, 2026Sep 3, 2026
Ameripharma Labs Limited Liability CompanyPHENYLEPHRINE HYDROCHLORIDE 3.5 mg/1; CHLORPHENIRAMINE MALEATE 10 mg/1Aug 8, 2026Aug 15, 2026

Roster from daily NDC Directory diffs — first/last seen dates start July 2026.

Cite this page

DrugDashboards, "PhenylephrineHydrochloride,CHLORPHENIRAMINEMALEATE — NDC 79706-0003-01," retrieved September 3, 2026, https://drugdashboards.com/drug/79706000301.

Free to cite with attribution — see how the data is put together.