NDC codes

FDA NDC Directory
Product NDC (as listed)72657-157Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72657-0157Add 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
72657-157-05726570157051 BOTTLE in 1 CARTON (72657-157-05) / 500 TABLET, FILM COATED in 1 BOTTLEMarketed from May 7, 2024
72657-157-18726570157181 BOTTLE in 1 CARTON (72657-157-18) / 18 TABLET, FILM COATED in 1 BOTTLEMarketed from May 7, 2024
72657-157-20726570157201 BOTTLE in 1 CARTON (72657-157-20) / 250 TABLET, FILM COATED in 1 BOTTLEMarketed from May 7, 2024
72657-157-36726570157361 BOTTLE in 1 CARTON (72657-157-36) / 36 TABLET, FILM COATED in 1 BOTTLEMarketed from May 7, 2024
72657-157-72726570157721 BOTTLE in 1 CARTON (72657-157-72) / 72 TABLET, FILM COATED in 1 BOTTLEMarketed from May 7, 2024
72657-157-74726570157741 BOTTLE in 1 CARTON (72657-157-74) / 144 TABLET, FILM COATED in 1 BOTTLEMarketed from May 7, 2024
72657-157-76726570157761 BOTTLE in 1 CARTON (72657-157-76) / 216 TABLET, FILM COATED in 1 BOTTLEMarketed from May 7, 2024

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, Ibuprofen
Generic name (nonproprietary)
acetaminophen, ibuprofen
Active ingredients
Ibuprofen — 125 mg/1Acetaminophen — 250 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218311
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 72657-157_b3d8d869-735e-4720-8b2b-a3eacc92041fSPL ID b3d8d869-735e-4720-8b2b-a3eacc92041fSPL set ID 57a8dc2b-a3bc-49fa-b605-2330155bdbffRxCUI 2387532UNII WK2XYI10QM, 362O9ITL9DUPC 0372657157742

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

N472657015705 followed by a unit qualifier and the quantity

Package 72657-0157-05. 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 relieves minor aches and pains due to: o headache o toothache o backache o menstrual cramps o muscular aches o minor pain of arthritis

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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