Viorele NDC 68462-318

NDC codes

FDA NDC Directory

Product NDC (as listed)68462-318Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68462-0318Add 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
68462-318-29	68462031829	3 BLISTER PACK in 1 CARTON (68462-318-29) / 1 KIT in 1 BLISTER PACK (68462-318-84)Marketed from Apr 4, 2012

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Viorele
Generic name (nonproprietary): desogestrel and ethinyl estradiol and ethinyl estradiol
Dosage form: Kit
Labeler: Glenmark Pharmaceuticals Inc., USA
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 091346
Marketing start: Apr 4, 2012
Listing expires: Dec 31, 2027
Identifiers: Product ID 68462-318_985b7e31-558c-4e49-b6ff-a0951bc4a947SPL ID 985b7e31-558c-4e49-b6ff-a0951bc4a947SPL set ID 39988aa6-8f68-40e8-9bdd-c40a3bdaad61RxCUI 248310, 249357, 748797, 759743, 1252016

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N468462031829 followed by a unit qualifier and the quantity

Package 68462-0318-29. 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 Jan 31, 2026. This label includes a boxed warning.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 091346

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

FDA NDC Directory listings under ANDA 091346
Product	Strength	Form · route	Labeler	Product NDC
Vioreledesogestrel and ethinyl estradiol and ethinyl estradiol	—	Kit	A-S Medication Solutions	50090-1395