NDC codes

FDA NDC Directory
Product NDC (as listed)59651-691Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59651-0691Add 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
59651-691-0159651069101100 CAPSULE in 1 BOTTLE (59651-691-01)Marketed from Sep 5, 2023
59651-691-0559651069105500 CAPSULE in 1 BOTTLE (59651-691-05)Marketed from Sep 5, 2023

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)
Loperamide Hydrochloride
Generic name (nonproprietary)
loperamide hydrochloride
Active ingredients
Loperamide hydrochloride — 2 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218122
Marketing start
Listing expires
Other FDA classes
Opioid Agonists (Mechanism)
Identifiers
Product ID 59651-691_8d142533-4e87-4030-8fe9-4fc7473b0442SPL ID 8d142533-4e87-4030-8fe9-4fc7473b0442SPL set ID 8d142533-4e87-4030-8fe9-4fc7473b0442RxCUI 978006UNII 77TI35393CUPC 0359651691014
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

N459651069101 followed by a unit qualifier and the quantity

Package 59651-0691-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Loperamide hydrochloride capsules are indicated for the control and symptomatic relief of acute nonspecific diarrhea in patients 2 years of age and older and of chronic diarrhea in adults associated with inflammatory bowel disease. Loperamide hydrochloride capsules are also indicated for reducing the volume of discharge from ileostomies.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 218122

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

FDA NDC Directory listings under ANDA 218122
ProductStrengthForm · routeLabelerProduct NDC
Loperamide HydrochlorideLoperamide hydrochloride 2 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-3618
Loperamide HydrochlorideLoperamide hydrochloride 2 mg/1CapsuleOralA-S Medication Solutions50090-7398
Loperamide HydrochlorideLoperamide hydrochloride 2 mg/1CapsuleOralNorthStar Rx LLC72603-328
Loperamide HydrochlorideLoperamide hydrochloride 2 mg/1CapsuleOralRedpharm Drug67296-2172
Loperamide HydrochlorideLoperamide hydrochloride 2 mg/1CapsuleOralREMEDYREPACK INC.70518-4283
Loperamide HClLoperamide hydrochloride 2 mg/1CapsuleOralDirect_Rx72189-686
Loperamide HydrochlorideLoperamide hydrochloride 2 mg/1CapsuleOralMajor Pharmaceuticals0904-7472
Loperamide HydrochlorideLoperamide hydrochloride 2 mg/1CapsuleOralBryant Ranch Prepack71335-2571
Loperamide HydrochlorideLoperamide hydrochloride 2 mg/1CapsuleOralCoupler LLC67046-1676

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