Over-the-counter drug · ANDA
Non-Drowsy Allergy Relief (Fexofenadine hydrochloride) NDC 11673-621
Fexofenadine hydrochloride 180 mg/1 · Tablet · Oral · TARGET CORPORATION
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 11673-621-01 | 1167306210111673062101 | 1 BOTTLE in 1 CARTON (11673-621-01) / 150 TABLET in 1 BOTTLEMarketed from Aug 1, 2025 | |
| 11673-621-15 | 1167306211511673062115 | 3 BLISTER PACK in 1 CARTON (11673-621-15) / 5 TABLET in 1 BLISTER PACKMarketed from Aug 1, 2025 | |
| 11673-621-30 | 1167306213011673062130 | 1 BOTTLE in 1 CARTON (11673-621-30) / 30 TABLET in 1 BOTTLEMarketed from Aug 1, 2025 | |
| 11673-621-50 | 1167306215011673062150 | 150 TABLET in 1 BOTTLE (11673-621-50)Marketed from Aug 1, 2025 | |
| 11673-621-70 | 1167306217011673062170 | 1 BOTTLE in 1 CARTON (11673-621-70) / 70 TABLET in 1 BOTTLEMarketed from Aug 1, 2025 |
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)
- Non-Drowsy Allergy Relief
- Generic name (nonproprietary)
- fexofenadine hydrochloride
- Active ingredients
- Fexofenadine hydrochloride — 180 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- TARGET CORPORATIONNDC labeler code 11673
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 076502
- Marketing start
- Listing expires
- Other FDA classes
- Histamine H1 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 11673-621_d7eb1caf-eeff-10b7-c464-3592c8d7d0eeSPL ID d7eb1caf-eeff-10b7-c464-3592c8d7d0eeSPL set ID 3cf4b7fe-b1f7-b767-430a-655408f91753RxCUI 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
N411673062101followed by a unit qualifier and the quantityPackage 11673-0621-01. 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 itchy, watery eyes sneezing itching of the nose or throat
Excerpt only. Read the full label for complete information.
About NDC 11673-621
- What is NDC 11673-621?
- 11673-621 is the product NDC for Non-Drowsy Allergy Relief (fexofenadine hydrochloride), Fexofenadine hydrochloride 180 mg/1 tablet, listed with the FDA by TARGET CORPORATION. It has 5 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Non-Drowsy Allergy Relief (Fexofenadine hydrochloride).
- What is the active ingredient?
- Fexofenadine hydrochloride.
- Who is the labeler?
- TARGET CORPORATION, NDC labeler code 11673. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Non-Drowsy Allergy Relief?
- 2 other product NDCs are listed under this name. See all Non-Drowsy Allergy Relief NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Non-Drowsy Allergy Relief products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Non-Drowsy Allergy Reliefloratadine tablet | Loratadine 10 mg/1 | TabletOral | Lil' Drug Store Products, Inc. | 66715-8815 | 66715-8815-06 |
| non drowsy allergy reliefloratadine | Loratadine 10 mg/1 | Tablet, Orally disintegratingOral | Meijer Distribution Inc | 41250-890 | 41250-0890-65 |
Other NDCs under ANDA 076502
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Allergy Relieffexofenadine hydrochloride | Fexofenadine hydrochloride 180 mg/1 | TabletOral | Rite Aid Corporation | 11822-3698 |
| Allergy Relieffexofenadine hydrochloride | Fexofenadine hydrochloride 180 mg/1 | TabletOral | Safeway Inc | 21130-784 |
| Allergy Relieffexofenadine hydrochloride | Fexofenadine hydrochloride 180 mg/1 | TabletOral | Family Dollar Stores, Inc. | 55319-917 |
| Fexofenadine hydrochloride | Fexofenadine hydrochloride 60 mg/1 | TabletOral | Walgreens Company | 0363-0783 |
| Fexofenadine hydrochloride | Fexofenadine hydrochloride 180 mg/1 | TabletOral | KROGER COMPANY | 30142-878 |
| Fexofenadine hydrochloride | Fexofenadine hydrochloride 180 mg/1 | TabletOral | Dr. Reddy's Laboratories Inc. | 43598-809 |
| Fexofenadine Hydrochloride | Fexofenadine hydrochloride 60 mg/1 | TabletOral | Dr. Reddy's Laboratories Inc. | 43598-936 |
| Fexofenadine hydrochloride | Fexofenadine hydrochloride 30 mg/1 | TabletOral | Dr. Reddy's Laboratories Limited | 55111-782 |
| Fexofenadine hydrochloride | Fexofenadine hydrochloride 60 mg/1 | TabletOral | Dr. Reddy's Laboratories Limited | 55111-783 |
| Fexofenadine hydrochloride | Fexofenadine hydrochloride 180 mg/1 | TabletOral | Dr. Reddy's Laboratories Limited | 55111-784 |
| Fexofenadine hydrochloride | Fexofenadine hydrochloride 180 mg/1 | TabletOral | Dollar General | 55910-111 |
| Fexofenadine Hydrochloride | Fexofenadine hydrochloride 180 mg/1 | TabletOral | Chain Drug Marketing Associate | 63868-025 |
| Fexofenadine hydrochloride | Fexofenadine hydrochloride 60 mg/1 | TabletOral | BluePoint Laboratories | 68001-439 |
| Fexofenadine hydrochloride | Fexofenadine hydrochloride 180 mg/1 | TabletOral | BluePoint Laboratories | 68001-440 |
| Fexofenadine Hydrochloride | Fexofenadine hydrochloride 180 mg/1 | TabletOral | Chain Drug Consortium, LLC | 68016-995 |
| Fexofenadine Hydrochloride | Fexofenadine hydrochloride 180 mg/1 | TabletOral | Sam's West Inc. | 68196-107 |
| Fexofenadine Hydrochloride | Fexofenadine hydrochloride 180 mg/1 | TabletOral | CVS Health Corp. | 69842-052 |
| Fexofenadine Hydrochloride | Fexofenadine hydrochloride 180 mg/1 | TabletOral | Strategic Sourcing Services, LLC | 70677-1009 |
| Wal-Fexfexofenadine hydrochloride | Fexofenadine hydrochloride 180 mg/1 | TabletOral | Walgreens Company | 0363-0784 |