Plan B One-Step (levonorgestrel) NDC 69536-162

NDC codes

FDA NDC Directory

Product NDC (as listed)69536-162Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69536-0162Add 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
69536-162-88	69536016288	1 BLISTER PACK in 1 BOX, UNIT-DOSE (69536-162-88) / 1 TABLET in 1 BLISTER PACKMarketed from May 10, 2018
69536-162-99	69536016299	1 BLISTER PACK in 1 BOX, UNIT-DOSE (69536-162-99) / 1 TABLET in 1 BLISTER PACKMarketed from Aug 15, 2019

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): Plan B One-Step
Generic name (nonproprietary): levonorgestrel
Active ingredients: Levonorgestrel — 1.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Foundation Consumer Healthcare LLC
Product type: Over-the-counter drug
Marketing category: NDA — New Drug ApplicationApplication NDA 021998
Marketing start: May 10, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Inhibit Ovum Fertilization (Physiologic effect)Progesterone Congeners (Chemical structure)Progesterone Congeners (Chemical structure)
Identifiers: Product ID 69536-162_a0190797-2a39-47be-803b-bec877085166SPL ID a0190797-2a39-47be-803b-bec877085166SPL set ID 6ce6b40e-14ac-47bd-a648-ddf9e452e559RxCUI 483325, 858079UNII 5W7SIA7YZWUPC 0369536146195, 0369536162881
Pharmacologic class: Progestin; Progestin-containing Intrauterine Device

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

N469536016288 followed by a unit qualifier and the quantity

Package 69536-0162-88. 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 Jan 31, 2023.

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 NDA 021998

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

FDA NDC Directory listings under NDA 021998
Product	Strength	Form · route	Labeler	Product NDC
Afteralevonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Foundation Consumer Healthcare LLC	69536-103
Next Choice One Doselevonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Foundation Consumer Healthcare LLC	69536-133
Plan B One-Steplevonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Foundation Consumer Healthcare LLC	69536-146
Take Actionlevonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Foundation Consumer Healthcare LLC	69536-200
Plan B One-Steplevonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	A-S Medication Solutions	50090-5978