Xelria Fe NDC 70700-308

NDC codes

FDA NDC Directory

Product NDC (as listed)70700-308Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70700-0308Add 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
70700-308-85	70700030885	3 POUCH in 1 CARTON (70700-308-85) / 1 BLISTER PACK in 1 POUCH (70700-308-84) / 1 KIT in 1 BLISTER PACKMarketed from Jan 29, 2025

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): Xelria Fe
Generic name (nonproprietary): norethindrone and ethinyl estradiol and ferrous fumarate
Dosage form: Kit
Labeler: Xiromed LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202086
Marketing start: Jan 29, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 70700-308_07f67e07-e0fe-aac7-9599-349da0b58775SPL ID 07f67e07-e0fe-aac7-9599-349da0b58775SPL set ID 6cc0558e-bdda-f234-0f36-2297f18be577RxCUI 433718, 1095223, 1095224, 2703268

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

N470700030885 followed by a unit qualifier and the quantity

Package 70700-0308-85. 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 Oct 20, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

Xelria Fe is indicated for use by females of reproductive potential to prevent pregnancy. Xelria 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)

Other NDCs under ANDA 202086

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

FDA NDC Directory listings under ANDA 202086
Product	Strength	Form · route	Labeler	Product NDC
Norethindrone And Ethinyl Estradiol And Ferrous Fumarate	—	Kit	Mylan Pharmaceuticals Inc.	0378-7297