What is NDC 70710-1710?

70710-1710 is the product NDC for ketorolac tromethamine, Ketorolac tromethamine 10 mg/1 tablet, film coated, listed with the FDA by Zydus Pharmaceuticals (USA) Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Zydus Pharmaceuticals (USA) Inc., NDC labeler code 70710. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for ketorolac tromethamine?

183 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

ketorolac tromethamine NDC 70710-1710

NDC codes

FDA NDC Directory

Product NDC (as listed)70710-1710Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70710-1710Add 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
70710-1710-1	7071017100170710171001	100 TABLET, FILM COATED in 1 BOTTLE (70710-1710-1)Marketed from Nov 10, 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 tromethamine — 10 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Zydus Pharmaceuticals (USA) Inc.NDC labeler code 70710
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217038
Marketing start: Nov 10, 2022
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 70710-1710_80144a41-dfe6-4ba9-bb1b-f846873043eaSPL ID 80144a41-dfe6-4ba9-bb1b-f846873043eaSPL set ID ffd84ef3-26ed-4810-952b-4f0e913c5e32RxCUI 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

N470710171001 followed by a unit qualifier and the quantity

Package 70710-1710-01. 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 Aug 6, 2024. 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 and other treatment options before deciding to use ketorolac tromethamine tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals. Acute Pain in Adult Patients Ketorolac tromethamine tablets 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 are to be used only as continuation treatment, if necess…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70710-1710

What is NDC 70710-1710?: 70710-1710 is the product NDC for ketorolac tromethamine, Ketorolac tromethamine 10 mg/1 tablet, film coated, listed with the FDA by Zydus Pharmaceuticals (USA) Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: ketorolac tromethamine.
What is the active ingredient?: Ketorolac tromethamine.
Who is the labeler?: Zydus Pharmaceuticals (USA) Inc., NDC labeler code 70710. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for ketorolac tromethamine?: 183 other product NDCs are listed under this name. See all ketorolac tromethamine 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 ketorolac tromethamine NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ketorolac Tromethamine	Ketorolac tromethamine 60 mg/2mL	Injection, SolutionIntramuscular	Anthea Pharma Private Limited	83854-024	83854-0024-25
Ketorolac Tromethamine	Ketorolac tromethamine 30 mg/mL	Injection, SolutionIntramuscular, Intravenous	Anthea Pharma Private Limited	83854-022	83854-0022-25
Ketorolac Tromethamine	Ketorolac tromethamine 10 mg/1	Tablet, Film coatedOral	Amerisyn LLC	87564-018	87564-0018-10
ketorolac tromethamine	Ketorolac tromethamine 10 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4129	68788-4129-0268788-4129-03
Ketorolac Tromethamine	Ketorolac tromethamine 30 mg/mL	Injection, SolutionIntramuscular	Baxter Healthcare Corporation	43066-053	43066-0053-10
Ketorolac Tromethamine	Ketorolac tromethamine 15 mg/mL	Injection, SolutionIntramuscular, Intravenous	Baxter Healthcare Corporation	43066-049	43066-0049-10
Ketorolac Tromethamine	Ketorolac tromethamine 30 mg/mL	Injection, SolutionIntramuscular, Intravenous	Baxter Healthcare Corporation	43066-051	43066-0051-10
Ketorolac Tromethamine	Ketorolac tromethamine 10 mg/1	Tablet, Film coatedOral	Injecta Medcial LLC	87234-7695	87234-7695-02
Ketorolac Tromethamine	Ketorolac tromethamine 30 mg/mL	Injection, SolutionIntramuscular, Intravenous	Cardinal Health 107, LLC	55154-7833	55154-7833-05
Ketorolac Tromethamine	Ketorolac tromethamine 10 mg/1	Tablet, Film coatedOral	Injecta Medcial LLC	87234-7695	87234-7695-01

All 184 ketorolac tromethamine NDCs

Other NDCs under ANDA 217038

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

FDA NDC Directory listings under ANDA 217038
Product	Strength	Form · route	Labeler	Product NDC
ketorolac tromethamine	Ketorolac tromethamine 10 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7808
ketorolac tromethamine	Ketorolac tromethamine 10 mg/1	Tablet, Film coatedOral	Redpharm Drug	67296-2230
ketorolac tromethamine	Ketorolac tromethamine 10 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-2983
ketorolac tromethamine	Ketorolac tromethamine 10 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-3591
ketorolac tromethamine	Ketorolac tromethamine 10 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4129
ketorolac tromethamine	Ketorolac tromethamine 10 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4255
ketorolac tromethamine	Ketorolac tromethamine 10 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1747
ketorolac tromethamine	Ketorolac tromethamine 10 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-3084