NDC codes

FDA NDC Directory
Product NDC (as listed)85766-035Labeler and product segments. Claims need a package NDC.
Product NDC at billing width85766-0035Add 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
85766-035-00857660035001 TABLET, FILM COATED in 1 BOTTLE (85766-035-00)Marketed from Aug 17, 2026
85766-035-0185766003501100 TABLET, FILM COATED in 1 BOTTLE (85766-035-01)Marketed from Aug 7, 2025
85766-035-02857660035022 TABLET, FILM COATED in 1 BOTTLE (85766-035-02)Marketed from Aug 12, 2026
85766-035-06857660035066 TABLET, FILM COATED in 1 BOTTLE (85766-035-06)Marketed from Apr 5, 2026
85766-035-108576600351010 TABLET, FILM COATED in 1 BOTTLE (85766-035-10)Marketed from Aug 7, 2025
85766-035-148576600351414 TABLET, FILM COATED in 1 BOTTLE (85766-035-14)Marketed from Aug 7, 2025
85766-035-208576600352020 TABLET, FILM COATED in 1 BOTTLE (85766-035-20)Marketed from Aug 7, 2025
85766-035-308576600353030 TABLET, FILM COATED in 1 BOTTLE (85766-035-30)Marketed from Aug 7, 2025
85766-035-608576600356060 TABLET, FILM COATED in 1 BOTTLE (85766-035-60)Marketed from Aug 7, 2025
85766-035-908576600359090 TABLET, FILM COATED in 1 BOTTLE (85766-035-90)Marketed from Aug 7, 2025

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)
Ketorolac Tromethamine
Generic name (nonproprietary)
ketorolac tromethamine
Active ingredients
Ketorolac tromethamine — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074754
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 85766-035_59415973-3019-b12d-e063-6294a90a88d6SPL ID 59415973-3019-b12d-e063-6294a90a88d6SPL set ID 0749f61d-12e6-4280-8f41-bd4df81e7ae6RxCUI 834022UNII 4EVE5946BQ
Pharmacologic class
Cyclooxygenase Inhibitor; 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

N485766003500 followed by a unit qualifier and the quantity

Package 85766-0035-00. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carefully consider the potential benefits and risks of ketorolac tromethamine tablets, USP and other treatment options before deciding to use ketorolac tromethamine tablets, USP. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals. Acute Pain in Adult Patients Ketorolac tromethamine tablets, USP are indicated for the short-term (≤ 5 days) management of moderately severe acute pain that requires analgesia at the opioid level, usually in a postoperative setting. Therapy should always be initiated with IV or IM dosing of ketorolac tromethamine and ketorolac tromethamine tablets, USP are to be used only as continuation …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 074754

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

FDA NDC Directory listings under ANDA 074754
ProductStrengthForm · routeLabelerProduct NDC
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.66267-832
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-0601
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-904
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralTeva Pharmaceuticals USA, Inc.0093-0314
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-170
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-104
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-032
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-0048
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralProficient Rx LP63187-128
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0139
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.66267-418
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-2974

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