NDC codes

FDA NDC Directory
Product NDC (as listed)69953-517Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69953-0517Add 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 NDC11-digit (billing)PackageCopy
69953-517-0169953051701699530517011 BLISTER PACK in 1 CARTON (69953-517-01) / 1 mg in 1 BLISTER PACKMarketed from Jan 16, 2023

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)
Morning After
Generic name (nonproprietary)
levonorgestrel
Active ingredients
Levonorgestrel — 1.5 mg/1.5mg
Dosage form
Tablet
Route
Oral
Labeler
Rapha Pharmaceuticals, Inc.NDC labeler code 69953
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 205329
Marketing start
Listing expires
Other FDA classes
Inhibit Ovum Fertilization (Physiologic effect)Progesterone Congeners (Chemical structure)Progesterone Congeners (Chemical structure)
Identifiers
Product ID 69953-517_f0fabe80-87bc-9b65-e053-2995a90a582bSPL ID f0fabe80-87bc-9b65-e053-2995a90a582bSPL set ID f0fab784-3d28-35fb-e053-2995a90ab611RxCUI 483325, 1657617UNII 5W7SIA7YZW
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

N469953051701 followed by a unit qualifier and the quantity

Package 69953-0517-01. 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 .

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)

About NDC 69953-517

What is NDC 69953-517?
69953-517 is the product NDC for Morning After (levonorgestrel), Levonorgestrel 1.5 mg/1.5mg tablet, listed with the FDA by Rapha Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Morning After (Levonorgestrel).
What is the active ingredient?
Levonorgestrel.
Who is the labeler?
Rapha Pharmaceuticals, Inc., NDC labeler code 69953. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Morning After?
2 other product NDCs are listed under this name. See all Morning After NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Morning After NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Morning AfterlevonorgestrelLevonorgestrel 1.5 mg/1.5mgTabletOralRapha Pharmaceuticals, Inc.69953-51669953-0516-01
Morning AfterlevonorgestrelLevonorgestrel 1.5 mg/1.5mgTabletOralRapha Pharmaceuticals, Inc.69953-51569953-0515-01

Other NDCs under ANDA 205329

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

FDA NDC Directory listings under ANDA 205329
ProductStrengthForm · routeLabelerProduct NDC
LevonorgestrelLevonorgestrel 1.5 mg/1TabletOralXiromed LLC70700-164
Morning AfterlevonorgestrelLevonorgestrel 1.5 mg/1.5mgTabletOralRapha Pharmaceuticals, Inc.69953-516
PostDay One-SteplevonorgestrelLevonorgestrel 1.5 mg/1.5mgTabletOralRapha Pharmaceuticals, Inc.69953-617
PostDay One-SteplevonorgestrelLevonorgestrel 1.5 mg/1.5mgTabletOralRapha Pharmaceuticals, Inc.69953-618
PostDay One-SteplevonorgestrelLevonorgestrel 1.5 mg/1.5mgTabletOralRapha Pharmaceuticals, Inc.69953-628

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