NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4436Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4436Add 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
70518-4436-07051844360070518443600180 TABLET in 1 BOTTLE, PLASTIC (70518-4436-0)Marketed from Aug 13, 2025

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)
Hyoscyamine Sulfate
Generic name (nonproprietary)
hyoscyamine sulfate
Active ingredients
Hyoscyamine sulfate — .125 mg/1
Dosage form
Tablet
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 70518-4436_5b34cb9a-1fe9-bd47-e063-6394a90ad4abSPL ID 5b34cb9a-1fe9-bd47-e063-6394a90ad4ab

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

N470518443600 followed by a unit qualifier and the quantity

Package 70518-4436-00. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 70518-4436

What is NDC 70518-4436?
70518-4436 is the product NDC for Hyoscyamine Sulfate, Hyoscyamine sulfate .125 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Hyoscyamine Sulfate.
What is the active ingredient?
Hyoscyamine sulfate.
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 Hyoscyamine Sulfate?
28 other product NDCs are listed under this name. See all Hyoscyamine Sulfate 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 Hyoscyamine Sulfate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Hyoscyamine SulfateHyoscyamine sulfate .125 mg/1TabletOralGranulation Technology, Inc.63561-020363561-0203-01
Hyoscyamine SulfateHyoscyamine sulfate .125 mg/1Tablet, Orally disintegratingOralGranulation Technology, Inc.63561-019763561-0197-01
Hyoscyamine SulfateHyoscyamine sulfate .125 mg/1Tablet, Orally disintegratingOralPD-Rx Pharmaceuticals, Inc.72789-56372789-0563-01
Hyoscyamine SulfateHyoscyamine sulfate .125 mg/1TabletSublingualGranulation Technology, Inc.63561-020263561-0202-01
Hyoscyamine SulfateHyoscyamine sulfate .125 mg/1TabletOralWestminster Pharmaceuticals, LLC69367-67769367-0677-01
Hyoscyamine SulfateHyoscyamine sulfate .125 mg/1TabletOralProficient Rx LP82804-96582804-0965-3082804-0965-6082804-0965-64+3 more
Hyoscyamine sulfateHyoscyamine sulfate .125 mg/1Tablet, Orally disintegratingOralChartwell RX, LLC62135-85862135-0858-12
Hyoscyamine SulfateHyoscyamine sulfate .375 mg/1Tablet, Extended releaseOralPatrin Pharma, Inc.39328-05239328-0052-10
Hyoscyamine SulfateHyoscyamine sulfate .125 mg/1Tablet, Orally disintegratingOralPatrin Pharma, Inc.39328-04939328-0049-10
Hyoscyamine SulfateHyoscyamine sulfate .125 mg/1TabletOralPatrin Pharma, Inc.39328-05039328-0050-10

All 29 Hyoscyamine Sulfate NDCs

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