Over-the-counter drug · ANDA

My After Plan (levonorgestrel) NDC 51660-098

Levonorgestrel 1.5 mg/1 · Tablet · Oral · OHM LABORATORIES INC

NDC codes

FDA NDC Directory
Product NDC (as listed)51660-098Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51660-0098Add 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
51660-098-11516600098111 BLISTER PACK in 1 CARTON (51660-098-11) / 1 TABLET in 1 BLISTER PACKMarketed from Sep 1, 2026

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)
My After Plan
Generic name (nonproprietary)
levonorgestrel
Active ingredients
Levonorgestrel — 1.5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207660
Marketing start
Listing expires
Other FDA classes
Inhibit Ovum Fertilization (Physiologic effect)Progesterone Congeners (Chemical structure)Progesterone Congeners (Chemical structure)
Identifiers
Product ID 51660-098_5baed416-d001-7834-e063-6394a90a0966SPL ID 5baed416-d001-7834-e063-6394a90a0966
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

N451660009811 followed by a unit qualifier and the quantity

Package 51660-0098-11. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 207660

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

FDA NDC Directory listings under ANDA 207660
ProductStrengthForm · routeLabelerProduct NDC
Morning After PilllevonorgestrelLevonorgestrel 1.5 mg/1TabletOralCadence Health Inc73436-8292
RestartlevonorgestrelLevonorgestrel 1.5 mg/1TabletOralWinx Health Inc.80584-103
My ChoicelevonorgestrelLevonorgestrel 1.5 mg/1TabletOralOHM LABORATORIES INC51660-096
JulielevonorgestrelLevonorgestrel 1.5 mg/1TabletOralJulie Products Inc82791-335
LevonorgestrelLevonorgestrel 1.5 mg/1TabletOralNaari Pte Limited79929-016

Med-Code uses cookies for analytics and advertising. You can accept or reject them; the site works either way. Privacy Policy.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in
My After Plan (levonorgestrel) NDC 51660-098 | Med-Code