What is NDC 70677-1239?

70677-1239 is the product NDC for FEXOFENADINE HCl, Fexofenadine hydrochloride 180 mg/1 tablet, film coated, listed with the FDA by Strategic Sourcing Services, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

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 FEXOFENADINE HCl?

45 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

FEXOFENADINE HCl NDC 70677-1239 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70677-1239Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70677-1239Add 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 NDC	11-digit (billing)	Package	Copy
70677-1239-1	7067712390170677123901	100 TABLET, FILM COATED in 1 BOTTLE (70677-1239-1)Marketed from Feb 22, 2024

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

Brand name (proprietary): FEXOFENADINE HCl
Generic name (nonproprietary): fexofenadine hcl
Active ingredients: Fexofenadine hydrochloride — 180 mg/1
Dosage form: Tablet, Film coated
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 210137
Marketing start: Feb 22, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 70677-1239_498a79fc-c2a8-c5ea-e063-6294a90ab355SPL ID 498a79fc-c2a8-c5ea-e063-6294a90ab355SPL set ID 7a49f700-5892-404b-b81a-4a92c1928806RxCUI 997420UNII 2S068B75ZU
Pharmacologic class: Histamine-1 Receptor Antagonist

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

N470677123901 followed by a unit qualifier and the quantity

Package 70677-1239-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

About NDC 70677-1239

What is NDC 70677-1239?: 70677-1239 is the product NDC for FEXOFENADINE HCl, Fexofenadine hydrochloride 180 mg/1 tablet, film coated, listed with the FDA by Strategic Sourcing Services, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: FEXOFENADINE HCl.
What is the active ingredient?: Fexofenadine 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 FEXOFENADINE HCl?: 45 other product NDCs are listed under this name. See all FEXOFENADINE HCl NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other FEXOFENADINE HCl NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Fexofenadine HCL	Fexofenadine hydrochloride 60 mg/1	TabletOral	YYBA Corp	73581-010	73581-0010-0173581-0010-0673581-0010-10+1 more
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	Walmart Inc.	79903-358	79903-0358-3079903-0358-4579903-0358-90
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	Strategic Sourcing Services	70677-1256	70677-1256-0170677-1256-02
fexofenadine hcl	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	Aphena Pharma Solutions - Tennessee, LLC	71610-905	71610-0905-3071610-0905-5371610-0905-60+1 more
fexofenadine hcl	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	Radha Pharmaceuticals	77771-202	77771-0202-0177771-0202-0577771-0202-30
fexofenadine hcl	Fexofenadine hydrochloride 60 mg/1	Tablet, Film coatedOral	Radha Pharmaceuticals	77771-201	77771-0201-0177771-0201-05
Fexofenadine HCl	Fexofenadine hydrochloride 180 mg/1	TabletOral	Rite Aid	11822-7661	11822-7661-05
Fexofenadine HCl	Fexofenadine hydrochloride 60 mg/1	TabletOral	Rite Aid	11822-7652	11822-7652-04
Fexofenadine HCl	Fexofenadine hydrochloride 180 mg/1	TabletOral	Rite Aid	11822-7663	11822-7663-04
Fexofenadine HCl	Fexofenadine hydrochloride 180 mg/1	TabletOral	Rite Aid	11822-7660	11822-7660-0311822-7660-0711822-7660-09

All 46 FEXOFENADINE HCl NDCs

Other NDCs under ANDA 210137

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

FDA NDC Directory listings under ANDA 210137
Product	Strength	Form · route	Labeler	Product NDC
CVS Fexofenadine Hydrochloridefexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	CVS Pharmacy	51316-183
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Pioneer Life Sciences, LLC	72090-010
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	YYBA Corp	73581-027
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	NUVICARE LLC	84324-008
Gencare Hives Relieffexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Pioneer Life Sciences, LLC	72090-058
Nuvicare Hives Relieffexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	NUVICARE LLC	84324-031