NDC codes

FDA NDC Directory
Product NDC (as listed)0573-0133Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00573-0133Add 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
0573-0133-01005730133013000 PACKET in 1 CASE (0573-0133-01) / 2 TABLET, COATED in 1 PACKETMarketed from Aug 11, 2014
0573-0133-020057301330250 PACKET in 1 TRAY (0573-0133-02) / 2 TABLET, COATED in 1 PACKETMarketed from Jul 8, 2013
0573-0133-04005730133042 PACKET in 1 BLISTER PACK (0573-0133-04) / 2 TABLET, COATED in 1 PACKETMarketed from Jul 8, 2013
0573-0133-05005730133052 PACKET in 1 CARTON (0573-0133-05) / 2 TABLET, COATED in 1 PACKETMarketed from Jul 8, 2013
0573-0133-20005730133201 BOTTLE in 1 CARTON (0573-0133-20) / 20 TABLET, COATED in 1 BOTTLEMarketed from Jul 8, 2013
0573-0133-40005730133401 BOTTLE in 1 CARTON (0573-0133-40) / 40 TABLET, COATED in 1 BOTTLEMarketed from Jul 8, 2013
0573-0133-41005730133411 BOTTLE in 1 CARTON (0573-0133-41) / 40 TABLET, COATED in 1 BOTTLEMarketed from Aug 12, 2015
0573-0133-80005730133801 BOTTLE in 1 CARTON (0573-0133-80) / 80 TABLET, COATED in 1 BOTTLEMarketed from Jul 8, 2013
0573-0133-81005730133811 BOTTLE in 1 CARTON (0573-0133-81) / 100 TABLET, COATED in 1 BOTTLEMarketed from Jul 8, 2013
0573-0133-88005730133882 BOTTLE in 1 PACKAGE (0573-0133-88) / 120 TABLET, COATED in 1 BOTTLEMarketed from Jul 8, 2013
0573-0133-89005730133891 BOTTLE in 1 CARTON (0573-0133-89) / 160 TABLET, COATED in 1 BOTTLEMarketed from Jul 8, 2013
0573-0133-91005730133911 BOTTLE in 1 CARTON (0573-0133-91) / 180 TABLET, COATED in 1 BOTTLEMarketed from Dec 1, 2014

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)
Advil
Generic name (nonproprietary)
ibuprofen sodium
Active ingredients
Ibuprofen sodium — 256 mg/1
Dosage form
Tablet, Coated
Route
Oral
Product type
Over-the-counter drug
Marketing category
NDA — New Drug ApplicationApplication NDA 201803
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 0573-0133_40429ef4-846a-eb4c-e063-6394a90ab7a9SPL ID 40429ef4-846a-eb4c-e063-6394a90ab7a9SPL set ID 5be198b8-396e-4b44-8819-e2e3b5d2ad0eRxCUI 153008, 310965UNII RM1CE97Z4N

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

N400573013301 followed by a unit qualifier and the quantity

Package 00573-0133-01. 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)

Uses temporarily relieves minor aches and pains due to: headache toothache backache menstrual cramps the common cold muscular aches minor pain of arthritis temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 201803

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

FDA NDC Directory listings under NDA 201803
ProductStrengthForm · routeLabelerProduct NDC
Advilibuprofen sodiumIbuprofen sodium 256 mg/1Tablet, CoatedOralHaleon US Holdings LLC0573-0134
Advil Menstrual Painibuprofen sodiumIbuprofen sodium 256 mg/1Tablet, CoatedOralHaleon US Holdings LLC0573-0230

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