What is NDC 69238-1551?

69238-1551 is the product NDC for Femynor kit, listed with the FDA by Amneal Pharmaceuticals NY LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Femynor (Norgestimate and ethinyl estradiol).

Amneal Pharmaceuticals NY LLC, NDC labeler code 69238. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Femynor?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Femynor NDC 69238-1551 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)69238-1551Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69238-1551Add 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
69238-1551-6	69238155106	1 BLISTER PACK in 1 CARTON (69238-1551-6) / 1 KIT in 1 BLISTER PACKMarketed from Jun 15, 2016

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): Femynor
Generic name (nonproprietary): norgestimate and ethinyl estradiol
Dosage form: Kit
Labeler: Amneal Pharmaceuticals NY LLCNDC labeler code 69238
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203865
Marketing start: Jun 15, 2016
Listing expires: Dec 31, 2026
Identifiers: Product ID 69238-1551_a123a86f-1a2a-4e89-9627-1bbcf9f237d2SPL ID a123a86f-1a2a-4e89-9627-1bbcf9f237d2SPL set ID 59bce25b-ee2c-4f06-afff-e5141d063602RxCUI 240128, 748797, 749860, 1796922UPC 0369238155167

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

N469238155106 followed by a unit qualifier and the quantity

Package 69238-1551-06. 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 May 30, 2016. This label includes a boxed warning.

Indications (excerpt from the label)

Femynor Tablets are indicated for use by females of reproductive potential to prevent pregnancy [ see Clinical Studies (14) ]. Femynor are estrogen/progestin COCs, 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)

About NDC 69238-1551

What is NDC 69238-1551?: 69238-1551 is the product NDC for Femynor kit, listed with the FDA by Amneal Pharmaceuticals NY LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Femynor (Norgestimate and ethinyl estradiol).
Who is the labeler?: Amneal Pharmaceuticals NY LLC, NDC labeler code 69238. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Femynor?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Femynor (Norgestimate and ethinyl estradiol) NDC 69238-1551