Levonorgestrel NDC 69230-333

NDC codes

FDA NDC Directory

Product NDC (as listed)69230-333Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69230-0333Add 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
69230-333-32	69230033332	1 BLISTER PACK in 1 CARTON (69230-333-32) / 1 TABLET in 1 BLISTER PACKMarketed from Sep 30, 2025
69230-333-33	69230033333	2 BLISTER PACK in 1 CARTON (69230-333-33) / 1 TABLET in 1 BLISTER PACKMarketed from Sep 30, 2025
69230-333-34	69230033334	5 BLISTER PACK in 1 CARTON (69230-333-34) / 1 TABLET in 1 BLISTER PACKMarketed from Sep 30, 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): Levonorgestrel
Generic name (nonproprietary): levonorgestrel
Active ingredients: Levonorgestrel — 1.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Camber Consumer Care Inc
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219102
Marketing start: Sep 30, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Inhibit Ovum Fertilization (Physiologic effect)Progesterone Congeners (Chemical structure)Progesterone Congeners (Chemical structure)
Identifiers: Product ID 69230-333_4db0336d-c9a4-8f40-e063-6394a90ad24bSPL ID 4db0336d-c9a4-8f40-e063-6394a90ad24bSPL set ID 2e22d0c4-b308-4a02-b2b0-2c06fb91d1e5RxCUI 483325UNII 5W7SIA7YZW
Pharmacologic class: Progestin; Progestin-containing Intrauterine System

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 HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N469230033332 followed by a unit qualifier and the quantity

Package 69230-0333-32. 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 Mar 23, 2026.

Indications (excerpt from the label)

Use for women to reduce chance of pregnancy after unprotected sex (if a contraceptive failed or if you did not use birth control)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 219102

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

FDA NDC Directory listings under ANDA 219102
Product	Strength	Form · route	Labeler	Product NDC
Levonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	YYBA CORP	73581-017