NDC codes

FDA NDC Directory
Product NDC (as listed)51316-585Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51316-0585Add 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
51316-585-3051316058530513160585301 BLISTER PACK in 1 CARTON (51316-585-30) / 28 TABLET in 1 BLISTER PACKMarketed from Jul 28, 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)
Daily Oral Contraceptive
Generic name (nonproprietary)
norgestrel
Active ingredients
Norgestrel — .075 mg/1
Dosage form
Tablet
Route
Oral
Product type
Over-the-counter drug
Marketing category
NDA — New Drug ApplicationApplication NDA 017031
Marketing start
Listing expires
Identifiers
Product ID 51316-585_2729baef-8caf-4c72-8899-fc1d76ebeb98SPL ID 2729baef-8caf-4c72-8899-fc1d76ebeb98SPL set ID 20477912-c1d6-4190-8f6e-00fb122134a1RxCUI 203717, 762335UNII 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

N451316058530 followed by a unit qualifier and the quantity

Package 51316-0585-30. 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 51316-585

What is NDC 51316-585?
51316-585 is the product NDC for Daily Oral Contraceptive (norgestrel), Norgestrel .075 mg/1 tablet, listed with the FDA by CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Daily Oral Contraceptive (Norgestrel).
What is the active ingredient?
Norgestrel.
Who is the labeler?
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED, NDC labeler code 51316. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Daily Oral Contraceptive?
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 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
NorgestrelNorgestrel .075 mg/1TabletOralWalgreen Company0363-5510
OpillnorgestrelNorgestrel .075 mg/1TabletOralL. Perrigo Company0113-8101
OpillnorgestrelNorgestrel .075 mg/1TabletOralRedpharm Drug67296-1938

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