NDC codes

FDA NDC Directory
Product NDC (as listed)59779-579Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59779-0579Add 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
59779-579-535977905795312 BLISTER PACK in 1 CARTON (59779-579-53) / 1 SUPPOSITORY in 1 BLISTER PACKMarketed from Jan 21, 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)
fever reducing childrensSuffix: childrens
Generic name (nonproprietary)
acetaminophen
Active ingredients
Acetaminophen — 120 mg/1
Dosage form
Suppository
Route
Rectal
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 070607
Marketing start
Listing expires
Identifiers
Product ID 59779-579_49e606bc-7b5f-4e1e-895c-fcfb92b46f8fSPL ID 49e606bc-7b5f-4e1e-895c-fcfb92b46f8fSPL set ID 9d89544f-3a66-4f23-b609-381d027e0c95RxCUI 198434UNII 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

N459779057953 followed by a unit qualifier and the quantity

Package 59779-0579-53. 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)

Other NDCs under ANDA 070607

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

FDA NDC Directory listings under ANDA 070607
ProductStrengthForm · routeLabelerProduct NDC
acetaminophen for childrenacetaminophenAcetaminophen 120 mg/1SuppositoryRectalPadagis Israel Pharmaceuticals Ltd45802-732
Foster and Thrive Pain RelieveracetaminophenAcetaminophen 120 mg/1SuppositoryRectalStrategic Sourcing Services LLC70677-1270
pain reliever fever reducer childrensacetaminophenAcetaminophen 120 mg/1SuppositoryRectalWalgreen Company0363-0579
acetaminophen for childrenacetaminophenAcetaminophen 120 mg/1SuppositoryRectalProficient Rx LP63187-373
acetaminophen for childrenacetaminophenAcetaminophen 120 mg/1SuppositoryRectalA-S Medication Solutions50090-0001
acetaminophen for childrenacetaminophenAcetaminophen 120 mg/1SuppositoryRectalNuCare Pharmaceutiacals,Inc.68071-4151
acetaminophen for childrenacetaminophenAcetaminophen 120 mg/1SuppositoryRectalNuCare Pharmaceuticals,Inc.68071-4172

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