Hyoscyamine Sulfate NDC 70518-4436

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 NDC	11-digit (billing)	Package	Copy
70518-4436-0	70518443600	180 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.
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Aug 13, 2025
Listing expires: Dec 31, 2027
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.