NDC codes

FDA NDC Directory
Product NDC (as listed)45802-730Labeler and product segments. Claims need a package NDC.
Product NDC at billing width45802-0730Add 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
45802-730-0045802073000458020730001 SUPPOSITORY in 1 BLISTER PACK (45802-730-00)Marketed from Oct 28, 2010
45802-730-30458020730304580207303012 BLISTER PACK in 1 CARTON (45802-730-30) / 1 SUPPOSITORY in 1 BLISTER PACKMarketed from Oct 28, 2010
45802-730-32458020730324580207303250 BLISTER PACK in 1 CARTON (45802-730-32) / 1 SUPPOSITORY in 1 BLISTER PACKMarketed from Nov 22, 2010
45802-730-334580207303345802073033100 BLISTER PACK in 1 CARTON (45802-730-33) / 1 SUPPOSITORY in 1 BLISTER PACKMarketed from Oct 28, 2010

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)
acetaminophen pain reliever fever reducerSuffix: pain reliever fever reducer
Generic name (nonproprietary)
acetaminophen
Active ingredients
Acetaminophen — 650 mg/1
Dosage form
Suppository
Route
Rectal
Labeler
Padagis Israel Pharmaceuticals LtdNDC labeler code 45802
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 070608
Marketing start
Marketing end
Identifiers
Product ID 45802-730_4926c350-ee6f-446c-a63d-cc7170f9a68cSPL ID 4926c350-ee6f-446c-a63d-cc7170f9a68cSPL set ID b43974c3-4db9-4201-beee-b22596a2b241RxCUI 198443UNII 362O9ITL9D

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N445802073000 followed by a unit qualifier and the quantity

Package 45802-0730-00. 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)

Uses temporarily • reduces fever • relieves minor aches, pains, and headache

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 45802-730

What is NDC 45802-730?
45802-730 is the product NDC for acetaminophen pain reliever fever reducer, Acetaminophen 650 mg/1 suppository, listed with the FDA by Padagis Israel Pharmaceuticals Ltd. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
acetaminophen pain reliever fever reducer (Acetaminophen).
What is the active ingredient?
Acetaminophen.
Who is the labeler?
Padagis Israel Pharmaceuticals Ltd, NDC labeler code 45802. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for acetaminophen pain reliever fever reducer?
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 070608

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

FDA NDC Directory listings under ANDA 070608
ProductStrengthForm · routeLabelerProduct NDC
foster and thrive pain relieveracetaminophenAcetaminophen 650 mg/1SuppositoryRectalStrategic Sourcing Services LLC70677-1271

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