Megestrol Acetate NDC 70518-4640

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4640Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4640Add 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
70518-4640-0	70518464000	50 POUCH in 1 BOX (70518-4640-0) / 1 TABLET in 1 POUCH (70518-4640-1)Marketed from Apr 27, 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): Megestrol Acetate
Generic name (nonproprietary): megestrol acetate
Active ingredients: Megestrol acetate — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: REMEDYREPACK INC.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 072422
Marketing start: Apr 27, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Progesterone Congeners (Chemical structure)
Identifiers: Product ID 70518-4640_5bc7cb1c-6fbb-9665-e063-6294a90aceb9SPL ID 5bc7cb1c-6fbb-9665-e063-6294a90aceb9
Pharmacologic class: Progestin

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

N470518464000 followed by a unit qualifier and the quantity

Package 70518-4640-00. 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.

Other NDCs under ANDA 072422

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

FDA NDC Directory listings under ANDA 072422
Product	Strength	Form · route	Labeler	Product NDC
Megestrol Acetate	Megestrol acetate 20 mg/1	TabletOral	Strides Pharma Science Limited	64380-158