What is NDC 70518-4283?

70518-4283 is the product NDC for Loperamide Hydrochloride, Loperamide hydrochloride 2 mg/1 capsule, listed with the FDA by REMEDYREPACK INC.. It has 6 package NDCs, shown above in 10- and 11-digit form.

REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Loperamide Hydrochloride?

74 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Loperamide Hydrochloride NDC 70518-4283

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4283Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4283Add 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
70518-4283-0	7051842830070518428300	30 CAPSULE in 1 BLISTER PACK (70518-4283-0)Marketed from Feb 10, 2025
70518-4283-1	7051842830170518428301	30 CAPSULE in 1 BLISTER PACK (70518-4283-1)Marketed from Feb 14, 2025
70518-4283-2	7051842830270518428302	15 CAPSULE in 1 BLISTER PACK (70518-4283-2)Marketed from Apr 1, 2025
70518-4283-3	7051842830370518428303	10 CAPSULE in 1 BLISTER PACK (70518-4283-3)Marketed from Apr 7, 2025
70518-4283-4	7051842830470518428304	20 CAPSULE in 1 BOTTLE, PLASTIC (70518-4283-4)Marketed from Aug 5, 2026
70518-4283-5	7051842830570518428305	50 POUCH in 1 BOX (70518-4283-5) / 1 CAPSULE in 1 POUCH (70518-4283-6)Marketed from Aug 7, 2026

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): Loperamide Hydrochloride
Generic name (nonproprietary): loperamide hydrochloride
Active ingredients: Loperamide hydrochloride — 2 mg/1
Dosage form: Capsule
Route: Oral
Labeler: REMEDYREPACK INC.NDC labeler code 70518
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218122
Marketing start: Feb 10, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Opioid Agonists (Mechanism)
Identifiers: Product ID 70518-4283_58786381-0bef-7a0c-e063-6394a90a99c5SPL ID 58786381-0bef-7a0c-e063-6394a90a99c5SPL set ID 3fdfc0e5-56a2-48a0-8ee6-390a194a29f3RxCUI 978006UNII 77TI35393C
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

N470518428300 followed by a unit qualifier and the quantity

Package 70518-4283-00. 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 Aug 7, 2026. 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)

About NDC 70518-4283

What is NDC 70518-4283?: 70518-4283 is the product NDC for Loperamide Hydrochloride, Loperamide hydrochloride 2 mg/1 capsule, listed with the FDA by REMEDYREPACK INC.. It has 6 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Loperamide Hydrochloride.
What is the active ingredient?: Loperamide hydrochloride.
Who is the labeler?: REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Loperamide Hydrochloride?: 74 other product NDCs are listed under this name. See all Loperamide Hydrochloride 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 Loperamide Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	Capsule, Liquid filledOral	YYBA CORP	73581-177	73581-0177-02
Loperamide Hydrochlorideloperamide hcl	Loperamide hydrochloride 1 mg/7.5mL	SolutionOral	Amazon.com Services LLC	72288-048	72288-0048-34
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	TabletOral	YYBA CORP	73581-175	73581-0175-24
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	CapsuleOral	Cardinal Health 107, LLC	55154-0277	55154-0277-00
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	TabletOral	Aurobindo Pharma Limited	84386-117	84386-0117-24
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	CapsuleOral	Coupler LLC	67046-1676	67046-1676-03
Loperamide Hydrochloride	Loperamide hydrochloride 1 mg/7.5mL	SolutionOral	DOLGENCORP INC	55910-155	55910-0155-55
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	CapsuleOral	Safecor Health LLC	48433-063	48433-0063-20
Loperamide Hydrochlorideloperamide hydrochloride oral	Loperamide hydrochloride 1 mg/7.5mL	SolutionOral	Bionpharma Inc.	69452-405	69452-0405-5569452-0405-93
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	TabletOral	Sportpharm LLC	85766-154	85766-0154-0685766-0154-12

All 75 Loperamide Hydrochloride NDCs

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
Product	Strength	Form · route	Labeler	Product NDC
Loperamide HCl	Loperamide hydrochloride 2 mg/1	CapsuleOral	Direct_Rx	72189-686
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	CapsuleOral	Major Pharmaceuticals	0904-7472
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	CapsuleOral	A-S Medication Solutions	50090-7398
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	CapsuleOral	Aurobindo Pharma Limited	59651-691
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	CapsuleOral	Coupler LLC	67046-1676
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	CapsuleOral	Redpharm Drug	67296-2172
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	CapsuleOral	NuCare Pharmaceuticals,Inc.	68071-3618
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	CapsuleOral	NuCare Pharmaceuticals,Inc.	68071-5331
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-2571
Loperamide Hydrochloride	Loperamide hydrochloride 2 mg/1	CapsuleOral	NorthStar Rx LLC	72603-328