Etonogestrel/Ethinyl Estradiol NDC 50090-5959

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-5959Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-5959Add 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
50090-5959-0	50090595900	1 POUCH in 1 BOX (50090-5959-0) / 1 d in 1 POUCHMarketed from Apr 7, 2022

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): Etonogestrel/Ethinyl Estradiol
Generic name (nonproprietary): etonogestrel and ethinyl estradiol
Active ingredients: Etonogestrel — .12 mg/dEthinyl estradiol — .015 mg/d
Dosage form: Insert, Extended release
Route: Vaginal
Labeler: A-S Medication Solutions
Product type: Prescription drug
Marketing category: NDA authorized genericApplication NDA 021187
Marketing start: Jun 1, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Estrogen Receptor Agonists (Mechanism)Progesterone Congeners (Chemical structure)
Identifiers: Product ID 50090-5959_74985d3b-59fe-491b-bf40-962faa0274abSPL ID 74985d3b-59fe-491b-bf40-962faa0274abSPL set ID fcf9da2a-bb91-4697-bfaa-c9d58855e275UNII 304GTH6RNH, 423D2T571U
Pharmacologic class: Estrogen; 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 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

N450090595900 followed by a unit qualifier and the quantity

Package 50090-5959-00. 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

Current FDA label (SPL), effective Nov 22, 2023. This label includes a boxed warning.

Indications (excerpt from the label)

FOR VAGINAL USE ONLY Etonogestrel/Ethinyl Estradiol Vaginal Ring is indicated for use by females of reproductive age to prevent pregnancy. Etonogestrel/Ethinyl Estradiol Vaginal Ring is an estrogen/progestin combination hormonal contraceptive (CHC) indicated for use by women to prevent pregnancy. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 021187

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

FDA NDC Directory listings under NDA 021187
Product	Strength	Form · route	Labeler	Product NDC
Nuvaringetonogestrel and ethinyl estradiol	Etonogestrel .12 mg/d; Ethinyl estradiol .015 mg/d	Insert, Extended releaseVaginal	A-S Medication Solutions	50090-7663
NuvaRingetonogestrel and ethinyl estradiol	Etonogestrel .12 mg/d; Ethinyl estradiol .015 mg/d	Insert, Extended releaseVaginal	Organon LLC	78206-146
Nuvaringetonogestrel and ethinyl estradiol	Etonogestrel .12 mg/d; Ethinyl estradiol .015 mg/d	Insert, Extended releaseVaginal	A-S Medication Solutions	50090-5611
NuvaRingetonogestrel and ethinyl estradiol	Etonogestrel .12 mg/d; Ethinyl estradiol .015 mg/d	Insert, Extended releaseVaginal	Advanz Pharma (US) Corp.	59212-146
Etonogestrel/Ethinyl Estradioletonogestrel and ethinyl estradiol	Etonogestrel .12 mg/d; Ethinyl estradiol .015 mg/d	Insert, Extended releaseVaginal	Prasco Laboratories	66993-605