What is NDC 62756-723?

62756-723 is the product NDC for AfterPlan (levonorgestrel), Levonorgestrel 1.5 mg/1 tablet, listed with the FDA by SUN PHARMACEUTICAL INDUSTRIES, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

SUN PHARMACEUTICAL INDUSTRIES, INC., NDC labeler code 62756. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for AfterPlan?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

AfterPlan NDC 62756-723 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62756-723Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62756-0723Add 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
62756-723-60	6275607236062756072360	1 BLISTER PACK in 1 CARTON (62756-723-60) / 1 TABLET in 1 BLISTER PACKMarketed from May 12, 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): AfterPlan
Generic name (nonproprietary): levonorgestrel
Active ingredients: Levonorgestrel — 1.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: SUN PHARMACEUTICAL INDUSTRIES, INC.NDC labeler code 62756
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202635
Marketing start: May 12, 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 62756-723_f86715c5-932d-405d-b81d-286c86409b1eSPL ID f86715c5-932d-405d-b81d-286c86409b1eSPL set ID c30c7bc2-04fa-4590-96f5-5bcf4bba3f1aRxCUI 483325, 2047728UNII 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

N462756072360 followed by a unit qualifier and the quantity

Package 62756-0723-60. 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 Oct 26, 2018.

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 62756-723

What is NDC 62756-723?: 62756-723 is the product NDC for AfterPlan (levonorgestrel), Levonorgestrel 1.5 mg/1 tablet, listed with the FDA by SUN PHARMACEUTICAL INDUSTRIES, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: AfterPlan (Levonorgestrel).
What is the active ingredient?: Levonorgestrel.
Who is the labeler?: SUN PHARMACEUTICAL INDUSTRIES, INC., NDC labeler code 62756. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for AfterPlan?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

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
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.	51660-723
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

AfterPlan (Levonorgestrel) NDC 62756-723