NDC codes

FDA NDC Directory
Product NDC (as listed)0113-8101Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00113-8101Add 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
0113-8101-0100113810101001138101011 BLISTER PACK in 1 CARTON (0113-8101-01) / 28 TABLET in 1 BLISTER PACKMarketed from Mar 4, 2024
0113-8101-0300113810103001138101033 BLISTER PACK in 1 CARTON (0113-8101-03) / 28 TABLET in 1 BLISTER PACKMarketed from Mar 4, 2024
0113-8101-0400113810104001138101044 BLISTER PACK in 1 PACKAGE (0113-8101-04) / 28 TABLET in 1 BLISTER PACKMarketed from Mar 22, 2024
0113-8101-0600113810106001138101066 BLISTER PACK in 1 CARTON (0113-8101-06) / 28 TABLET in 1 BLISTER PACKMarketed from Mar 4, 2024

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Opill
Generic name (nonproprietary)
norgestrel
Active ingredients
Norgestrel — .075 mg/1
Dosage form
Tablet
Route
Oral
Labeler
L. Perrigo CompanyNDC labeler code 0113
Product type
Over-the-counter drug
Marketing category
NDA — New Drug ApplicationApplication NDA 017031
Marketing start
Listing expires
Identifiers
Product ID 0113-8101_fb2ad1e4-4e8a-4cee-a6e8-a823401dd8feSPL ID fb2ad1e4-4e8a-4cee-a6e8-a823401dd8feSPL set ID 69dfa2ac-6a7e-4587-929c-9acabd97973bRxCUI 203717, 762335, 2676107UNII 3J8Q1747Z2

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

N400113810101 followed by a unit qualifier and the quantity

Package 00113-8101-01. 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 To prevent pregnancy

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0113-8101

What is NDC 0113-8101?
0113-8101 is the product NDC for Opill (norgestrel), Norgestrel .075 mg/1 tablet, listed with the FDA by L. Perrigo Company. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Opill (Norgestrel).
What is the active ingredient?
Norgestrel.
Who is the labeler?
L. Perrigo Company, NDC labeler code 0113. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Opill?
1 other product NDC are listed under this name. See all Opill 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 Opill NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
OpillnorgestrelNorgestrel .075 mg/1TabletOralRedpharm Drug67296-193867296-1938-02

Other NDCs under NDA 017031

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

FDA NDC Directory listings under NDA 017031
ProductStrengthForm · routeLabelerProduct NDC
Daily Oral ContraceptivenorgestrelNorgestrel .075 mg/1TabletOralCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED51316-585
NorgestrelNorgestrel .075 mg/1TabletOralWalgreen Company0363-5510
OpillnorgestrelNorgestrel .075 mg/1TabletOralRedpharm Drug67296-1938

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