What is NDC 51660-723?

51660-723 is the product NDC for Levonorgestrel, Levonorgestrel 1.5 mg/1 tablet, listed with the FDA by Ohm Laboratories Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Ohm Laboratories Inc., NDC labeler code 51660. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Levonorgestrel?

11 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Levonorgestrel NDC 51660-723 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)51660-723Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51660-0723Add 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
51660-723-11	5166007231151660072311	1 BLISTER PACK in 1 CARTON (51660-723-11) / 1 TABLET in 1 BLISTER PACKMarketed from Nov 1, 2017

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: Ohm Laboratories Inc.NDC labeler code 51660
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202635
Marketing start: Nov 1, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Inhibit Ovum Fertilization (Physiologic effect)Progesterone Congeners (Chemical structure)Progesterone Congeners (Chemical structure)
Identifiers: Product ID 51660-723_8beab701-88ae-4dbb-9d89-844ef79dd098SPL ID 8beab701-88ae-4dbb-9d89-844ef79dd098SPL set ID 5c509934-8c11-4d7f-8506-5971c37cfc22RxCUI 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

N451660072311 followed by a unit qualifier and the quantity

Package 51660-0723-11. 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

Current FDA label (SPL), effective Sep 6, 2024.

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 51660-723

What is NDC 51660-723?: 51660-723 is the product NDC for Levonorgestrel, Levonorgestrel 1.5 mg/1 tablet, listed with the FDA by Ohm Laboratories Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Levonorgestrel.
What is the active ingredient?: Levonorgestrel.
Who is the labeler?: Ohm Laboratories Inc., NDC labeler code 51660. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Levonorgestrel?: 11 other product NDCs are listed under this name. See all Levonorgestrel 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 Levonorgestrel NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Levonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	YYBA CORP	73581-017	73581-0017-01
Levonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	YYBA Corp	73581-217	73581-0217-01
Levonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Camber Consumer Care Inc	69230-333	69230-0333-3269230-0333-3369230-0333-34
Levonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Thirty Madison Inc.	71713-098	71713-0098-11
Levonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	LEADER/ CARDINAL HEALTH 110, INC.	70000-0675	70000-0675-01
Levonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Rugby Laboratories	0536-1433	00536-1433-63
Levonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Naari Pte Limited	79929-016	79929-0016-01
Levonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	GLENMARK THERAPEUTICS INC., USA	72657-123	72657-0123-11
Levonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Xiromed LLC	70700-164	70700-0164-06
Levonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Ohm Laboratories Inc.	51660-999	51660-0999-0151660-0999-11

All 12 Levonorgestrel NDCs

Other NDCs under ANDA 202635

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

FDA NDC Directory listings under ANDA 202635
Product	Strength	Form · route	Labeler	Product NDC
AfterPlanlevonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	SUN PHARMACEUTICAL INDUSTRIES, INC.	62756-723
LEADER Emergency Contraceptive Levonorgestrellevonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Cardinal Health 110, LLC. DBA Leader	70000-0600
Levonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Ohm Laboratories Inc.	51660-999
Levonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Thirty Madison Inc.	71713-098
My Choice TMlevonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	SUN PHARMACEUTICAL INDUSTRIES, INC.	62756-720
My Choice TMlevonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Proficient Rx LP	71205-120
Opcicon One-Steplevonorgestrel	Levonorgestrel 1.5 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	62756-718