NDC codes

FDA NDC Directory
Product NDC (as listed)70677-1315Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70677-1315Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
70677-1315-1706771315017067713150120 BLISTER PACK in 1 CARTON (70677-1315-1) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Feb 11, 2026
70677-1315-2706771315027067713150230 BLISTER PACK in 1 CARTON (70677-1315-2) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Feb 11, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Generic name (nonproprietary)
fexofenadine hydrochloride, pseudoephedrine hydrochloride
Active ingredients
Fexofenadine hydrochloride — 60 mg/1Pseudoephedrine hydrochloride — 120 mg/1
Dosage form
Tablet, Film coated, Extended release
Route
Oral
Labeler
Strategic Sourcing Services LLCNDC labeler code 70677
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216792
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Agonists (Mechanism)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 70677-1315_5a743183-8c1e-458f-8a76-cf207553e6cbSPL ID 5a743183-8c1e-458f-8a76-cf207553e6cbSPL set ID 945fcda4-0dd8-43cf-a5dd-ecea7995330aRxCUI 997406UNII 2S068B75ZU, 6V9V2RYJ8NUPC 0010870000093
Pharmacologic class
Histamine-1 Receptor Antagonist; alpha-Adrenergic Agonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470677131501 followed by a unit qualifier and the quantity

Package 70677-1315-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Uses • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • sneezing • itchy, watery eyes • itching of the nose or throat • temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies • reduces swelling of nasal passages • temporarily relieves sinus congestion and pressure • temporarily restores freer breathing through the nose

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70677-1315

What is NDC 70677-1315?
70677-1315 is the product NDC for Foster And Thrive Allergy And Congestion D, Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1 tablet, film coated, extended release, listed with the FDA by Strategic Sourcing Services LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Foster And Thrive Allergy And Congestion D (Fexofenadine hydrochloride, pseudoephedrine hydrochloride).
What is the active ingredient?
Fexofenadine hydrochloride, Pseudoephedrine hydrochloride.
Who is the labeler?
Strategic Sourcing Services LLC, NDC labeler code 70677. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Foster And Thrive Allergy And Congestion D?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under ANDA 216792

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 216792
ProductStrengthForm · routeLabelerProduct NDC
Equate Allergy Relief Dfexofenadine hydrochloride, pseudoephedrine hydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralWALMART INC.79903-424
Leader 12Hr Allergy And Congestion Relieffexofenadine hydrochloride, pseudoephedrine hydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralCardinal Health 110, LLC. dba Leader70000-0772
Rugby Allergy Relief Dfexofenadine hydrochloride, pseudoephedrine hydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralRugby Laboratories0536-1491

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