Nexesta Fe NDC 65862-926

NDC codes

FDA NDC Directory

Product NDC (as listed)65862-926Labeler and product segments. Claims need a package NDC.

Product NDC at billing width65862-0926Add 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
65862-926-58	65862092658	5 POUCH in 1 CARTON (65862-926-58) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACKMarketed from Feb 2, 2017
65862-926-87	65862092687	1 POUCH in 1 CARTON (65862-926-87) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACKMarketed from Feb 2, 2017
65862-926-88	65862092688	3 POUCH in 1 CARTON (65862-926-88) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACKMarketed from Feb 2, 2017
65862-926-97	65862092697	72 POUCH in 1 CARTON (65862-926-97) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACKMarketed from Feb 2, 2017

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): Nexesta Fe
Generic name (nonproprietary): norethindrone and ethinyl estradiol and ferrous fumarate
Dosage form: Kit
Labeler: Aurobindo Pharma Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207535
Marketing start: Feb 2, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 65862-926_c442d603-f61f-4f9e-8776-15d764842c27SPL ID c442d603-f61f-4f9e-8776-15d764842c27SPL set ID 6eb8f7b6-4b8e-4bad-800a-b2f3b36c3413RxCUI 433718, 1095223, 1095224, 1869047

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

N465862092658 followed by a unit qualifier and the quantity

Package 65862-0926-58. 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 Dec 4, 2021. This label includes a boxed warning.

Indications (excerpt from the label)

Nexesta Fe is indicated for use by females of reproductive potential to prevent pregnancy. Nexesta Fe is a progestin/estrogen COC indicated for use by females of reproductive potential to prevent pregnancy. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)