NDC codes

FDA NDC Directory
Product NDC (as listed)70301-2017Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70301-2017Add 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
70301-2017-17030120170130 TABLET, COATED in 1 BOTTLE (70301-2017-1)Marketed from Sep 30, 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)
Exemestane
Generic name (nonproprietary)
exemestane
Active ingredients
Exemestane — 25 mg/1
Dosage form
Tablet, Coated
Route
Oral
Labeler
OPKO Pharmaceuticals, LLCNDC labeler code 70301
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 200898
Marketing start
Listing expires
Other FDA classes
Aromatase Inhibitors (Mechanism)
Identifiers
Product ID 70301-2017_59e4ab75-dde7-fbf1-e063-6394a90a8d04SPL ID 59e4ab75-dde7-fbf1-e063-6394a90a8d04
Pharmacologic class
Aromatase Inhibitor

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

N470301201701 followed by a unit qualifier and the quantity

Package 70301-2017-01. 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

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

About NDC 70301-2017

What is NDC 70301-2017?
70301-2017 is the product NDC for Exemestane, Exemestane 25 mg/1 tablet, coated, listed with the FDA by OPKO Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Exemestane.
What is the active ingredient?
Exemestane.
Who is the labeler?
OPKO Pharmaceuticals, LLC, NDC labeler code 70301. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Exemestane?
10 other product NDCs are listed under this name. See all Exemestane 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 Exemestane NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ExemestaneExemestane 25 mg/1Tablet, Film coatedOralNorthStar Rx LLC72603-32972603-0329-01
ExemestaneExemestane 25 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-51659651-0516-30
ExemestaneExemestane 25 mg/1Tablet, Film coatedOralFlorida Pharmaceutical Products, LLC71921-19071921-0190-33
ExemestaneExemestane 25 mg/1Tablet, Film coatedOralBreckenridge Pharmaceutical, Inc.51991-00551991-0005-90
ExemestaneExemestane 25 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-205663629-2056-01
ExemestaneExemestane 25 mg/1TabletOralZydus Pharmaceuticals USA Inc.68382-38368382-0383-06
ExemestaneExemestane 25 mg/1TabletOralZydus Lifesciences Limited70771-137470771-1374-03
ExemestaneExemestane 25 mg/1TabletOralCipla USA Inc.69097-31669097-0316-02
ExemestaneExemestane 25 mg/1TabletOralUpsher-Smith Laboratories, Inc.0832-059500832-0595-30
ExemestaneExemestane 25 mg/1Tablet, Sugar coatedOralMylan Pharmaceuticals Inc.59762-285859762-2858-01

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