Ibuprofen NDC 49035-693

NDC codes

FDA NDC Directory

Product NDC (as listed)49035-693Labeler and product segments. Claims need a package NDC.

Product NDC at billing width49035-0693Add 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
49035-693-08	49035069308	1 BOTTLE in 1 CARTON (49035-693-08) / 120 mL in 1 BOTTLEMarketed from Feb 14, 2019
49035-693-09	49035069309	1 BOTTLE in 1 CARTON (49035-693-09) / 120 mL in 1 BOTTLEMarketed from Mar 4, 2021

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: EQUATE (WAL-MART STORES, INC.)
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, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 49035-693_3bb4a859-a353-e550-e063-6394a90a7645SPL ID 3bb4a859-a353-e550-e063-6394a90a7645SPL set ID 104b5ac1-9c5e-40f8-a9b1-1761b495bb1cRxCUI 197803UNII WK2XYI10QMUPC 0681131433570
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

N449035069308 followed by a unit qualifier and the quantity

Package 49035-0693-08. 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 Aug 6, 2025.

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)

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
Ibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	Sun Pharmaceutical Industries, Inc.	51672-2130
Childrens Ibuprofenibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	Kroger Company	30142-965
Ibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	Sun Pharmaceutical Industries, Inc.	51672-2144
Ibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	HF Acquisition Co LLC, DBA HealthFirst	51662-1582
Ibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	Preferred Pharmaceuticals Inc.	68788-8288
Ibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	Proficient Rx LP	71205-213
Childrens Ibuprofenibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	Rite Aid Corporation	11822-9998
Ibuprofen	Ibuprofen 100 mg/5mL	SuspensionOral	A-S Medication Solutions	50090-7274