What is NDC 71205-213?

71205-213 is the product NDC for Ibuprofen, Ibuprofen 100 mg/5mL suspension, listed with the FDA by Proficient Rx LP. It has 1 package NDC, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Ibuprofen?

674 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ibuprofen NDC 71205-213 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-213Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0213Add 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 NDC	11-digit (billing)	Package	Copy
71205-213-72	7120502137271205021372	1 BOTTLE in 1 CARTON (71205-213-72) / 120 mL in 1 BOTTLEMarketed from Jan 1, 2019

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): Ibuprofen
Generic name (nonproprietary): ibuprofen
Active ingredients: Ibuprofen — 100 mg/5mL
Dosage form: Suspension
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 71205
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 209207
Marketing start: Jun 27, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 71205-213_caf36ae7-7d2e-4058-aa5b-35122c1187abSPL ID caf36ae7-7d2e-4058-aa5b-35122c1187abSPL set ID b7565aac-a928-4116-b9af-cf636da4537cRxCUI 197803UNII WK2XYI10QM
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

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

N471205021372 followed by a unit qualifier and the quantity

Package 71205-0213-72. 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 Jul 1, 2022.

Indications (excerpt from the label)

Uses temporarily: • relieves minor aches and pains due to the common cold, flu, sore throat, headache and toothache • reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-213

What is NDC 71205-213?: 71205-213 is the product NDC for Ibuprofen, Ibuprofen 100 mg/5mL suspension, listed with the FDA by Proficient Rx LP. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Ibuprofen.
What is the active ingredient?: Ibuprofen.
Who is the labeler?: Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ibuprofen?: 674 other product NDCs are listed under this name. See all Ibuprofen NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Ibuprofen NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4784	70518-4784-0070518-4784-01
Ibuprofen	Ibuprofen 400 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4786	70518-4786-00
Ibuprofen	Ibuprofen 200 mg/1	TabletOral	Famora Inc	87509-0004	87509-0004-05
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	Medcore LLC	82461-725	82461-0725-90
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	Medcore LLC	82461-724	82461-0724-90
Ibuprofen	Ibuprofen 200 mg/1	TabletOral	Aurohealth LLC	58602-913	58602-0913-1758602-0913-40
Ibuprofen	Ibuprofen 600 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-738	67877-0738-0167877-0738-0567877-0738-30+3 more
Ibuprofen	Ibuprofen 400 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-737	67877-0737-0167877-0737-0567877-0737-33+1 more
Ibuprofen	Ibuprofen 800 mg/1	Tablet, Film coatedOral	Ascend Laboratories, LLC	67877-739	67877-0739-0167877-0739-0567877-0739-30+4 more
Ibuprofen	Ibuprofen 200 mg/1	Capsule, Liquid filledOral	GOODSENSE	50804-185	50804-0185-0150804-0185-02

All 675 Ibuprofen NDCs

Other NDCs under ANDA 209207

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

FDA NDC Directory listings under ANDA 209207
Product	Strength	Form · route	Labeler	Product NDC
Childrens Ibuprofenibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	Rite Aid Corporation	11822-9998
Childrens Ibuprofenibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	Kroger Company	30142-965
Ibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	EQUATE (WAL-MART STORES, INC.)	49035-693
Ibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	A-S Medication Solutions	50090-7274
Ibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	HF Acquisition Co LLC, DBA HealthFirst	51662-1582
Ibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	Sun Pharmaceutical Industries, Inc.	51672-2130
Ibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	Sun Pharmaceutical Industries, Inc.	51672-2144
Ibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	Preferred Pharmaceuticals Inc.	68788-8288