NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2136Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2136Add 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
71335-2136-0713352136003 TABLET, FILM COATED in 1 BOTTLE (71335-2136-0)Marketed from Aug 2, 2022
71335-2136-17133521360130 TABLET, FILM COATED in 1 BOTTLE (71335-2136-1)Marketed from Aug 2, 2022
71335-2136-27133521360210 TABLET, FILM COATED in 1 BOTTLE (71335-2136-2)Marketed from Aug 2, 2022
71335-2136-37133521360320 TABLET, FILM COATED in 1 BOTTLE (71335-2136-3)Marketed from Aug 2, 2022
71335-2136-47133521360490 TABLET, FILM COATED in 1 BOTTLE (71335-2136-4)Marketed from Aug 2, 2022
71335-2136-57133521360516 TABLET, FILM COATED in 1 BOTTLE (71335-2136-5)Marketed from Aug 2, 2022
71335-2136-6713352136068 TABLET, FILM COATED in 1 BOTTLE (71335-2136-6)Marketed from Aug 2, 2022
71335-2136-77133521360715 TABLET, FILM COATED in 1 BOTTLE (71335-2136-7)Marketed from Aug 2, 2022
71335-2136-8713352136085 TABLET, FILM COATED in 1 BOTTLE (71335-2136-8)Marketed from Aug 2, 2022
71335-2136-971335213609100 TABLET, FILM COATED in 1 BOTTLE (71335-2136-9)Marketed from Aug 2, 2022

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 tromethamine10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215788
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 71335-2136_f1d92737-780f-4c36-a655-ca478c850a4bSPL ID f1d92737-780f-4c36-a655-ca478c850a4bSPL set ID 9e5fde54-2206-4072-afb8-4d06a8d314b1RxCUI 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

N471335213600 followed by a unit qualifier and the quantity

Package 71335-2136-00. 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 trea

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 215788

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

FDA NDC Directory listings under ANDA 215788
ProductStrengthForm · routeLabelerProduct NDC
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2658
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-7303
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7638
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralAmerisyn LLC87564-018
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralRedpharm Drug67296-2163
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC82868-020
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0267
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7453
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8891
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralAjanta Pharma USA Inc.27241-316
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-677
Ketorolac TromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralDR. REDDY'S LABORATORIES, INC.43598-139
ketorolac tromethamineKetorolac tromethamine 10 mg/1Tablet, Film coatedOralAmici Pharma Inc.69292-650

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