Over-the-counter drug · ANDA
Anti-Diarrheal (loperamide hydrochloride) NDC 41226-797
Loperamide hydrochloride 2 mg/1 · Tablet, Film coated · Oral · Kroger
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 41226-797-22 | 41226079722 | 2 BLISTER PACK in 1 CARTON (41226-797-22) / 6 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Sep 18, 2026 | |
| 41226-797-24 | 41226079724 | 4 BLISTER PACK in 1 CARTON (41226-797-24) / 6 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Sep 18, 2026 |
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)
- Anti-Diarrheal
- Generic name (nonproprietary)
- loperamide hydrochloride
- Active ingredients
- Loperamide hydrochloride — 2 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Kroger
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 220153
- Marketing start
- Listing expires
- Other FDA classes
- Opioid Agonists (Mechanism)
- Identifiers
- Product ID 41226-797_5a2a774a-a0fe-cf2c-e063-6294a90a29faSPL ID 5a2a774a-a0fe-cf2c-e063-6294a90a29fa
- Pharmacologic class
- Opioid 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
N441226079722followed by a unit qualifier and the quantityPackage 41226-0797-22. 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
The FDA listing for this product does not reference a label (SPL) set.