What is NDC 37808-022?

37808-022 is the product NDC for Fexofenadine HCl and Pseudoephedrine HCI, Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1 tablet, extended release, listed with the FDA by HEB. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Fexofenadine hydrochloride, Pseudoephedrine hydrochloride.

HEB, NDC labeler code 37808. 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 and Pseudoephedrine HCI?

7 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 and Pseudoephedrine HCI NDC 37808-022

NDC codes

FDA NDC Directory

Product NDC (as listed)37808-022Labeler and product segments. Claims need a package NDC.

Product NDC at billing width37808-0022Add 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
37808-022-31	3780800223137808002231	6 BLISTER PACK in 1 CARTON (37808-022-31) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Dec 21, 2015

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 and Pseudoephedrine HCI
Generic name (nonproprietary): fexofenadine hcl and pseudoephedrine hci
Active ingredients: Fexofenadine hydrochloride — 60 mg/1Pseudoephedrine hydrochloride — 120 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: HEBNDC labeler code 37808
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076667
Marketing start: Dec 21, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 37808-022_8c74b0a5-6bbc-0f8d-bbda-46d6cb39aea6SPL ID 8c74b0a5-6bbc-0f8d-bbda-46d6cb39aea6SPL set ID 0de7fc37-7f46-4e98-d5ac-d31a3c313a62RxCUI 997406UNII 2S068B75ZU, 6V9V2RYJ8N
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

N437808002231 followed by a unit qualifier and the quantity

Package 37808-0022-31. 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 Dec 7, 2017.

Indications (excerpt from the label)

Use(s) temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing nasal congestion itchy, watery eyes itching of the nose or throat 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 37808-022

What is NDC 37808-022?: 37808-022 is the product NDC for Fexofenadine HCl and Pseudoephedrine HCI, Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1 tablet, extended release, listed with the FDA by HEB. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Fexofenadine HCl and Pseudoephedrine HCI.
What is the active ingredient?: Fexofenadine hydrochloride, Pseudoephedrine hydrochloride.
Who is the labeler?: HEB, NDC labeler code 37808. 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 and Pseudoephedrine HCI?: 7 other product NDCs are listed under this name. See all Fexofenadine HCl and Pseudoephedrine HCI 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 and Pseudoephedrine HCI NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Fexofenadine HCl and Pseudoephedrine HCI	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	Walgreens Company	0363-1606	00363-1606-2000363-1606-30
Fexofenadine HCl and Pseudoephedrine HCI	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	Dr. Reddy's Laboratories Inc.	43598-823	43598-0823-1443598-0823-3143598-0823-35
Fexofenadine HCl and Pseudoephedrine HCI	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	The Kroger Co.	30142-611	30142-0611-14
Fexofenadine HCl and Pseudoephedrine HCI	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	The Kroger Co.	30142-447	30142-0447-14
Fexofenadine HCl and Pseudoephedrine HCI	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	CVS Pharmacy	59779-508	59779-0508-1459779-0508-31
Fexofenadine HCl and Pseudoephedrine HCI	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	Dr. Reddy's Laboratories Limited	55111-447	55111-0447-1455111-0447-3155111-0447-35
Fexofenadine HCl and Pseudoephedrine HCI	Fexofenadine hydrochloride 180 mg/1; Pseudoephedrine hydrochloride 240 mg/1	Tablet, Extended releaseOral	Dr.Reddy's Laboratories Limited	55111-557	55111-0557-0755111-0557-2955111-0557-35

Other NDCs under ANDA 076667

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

FDA NDC Directory listings under ANDA 076667
Product	Strength	Form · route	Labeler	Product NDC
Allergy and Congestionfexofenadine hcl and pseudoephedrine hci	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	Rite Aid Corporation	11822-7388
Fexofenadine HCl and Pseudoephedrine HCI	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	Walgreens Company	0363-1606
Fexofenadine HCl and Pseudoephedrine HCI	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	The Kroger Co.	30142-447
Fexofenadine HCl and Pseudoephedrine HCI	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	The Kroger Co.	30142-611
Fexofenadine HCl and Pseudoephedrine HCI	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	Dr. Reddy's Laboratories Inc.	43598-823
Fexofenadine HCl and Pseudoephedrine HCI	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	Dr. Reddy's Laboratories Limited	55111-447
Fexofenadine HCl and Pseudoephedrine HCI	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	CVS Pharmacy	59779-508