NDC codes

FDA NDC Directory
Product NDC (as listed)71335-0070Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-0070Add 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
71335-0070-0713350070007 TABLET in 1 BOTTLE (71335-0070-0)Marketed from Jun 28, 2022
71335-0070-17133500700114 TABLET in 1 BOTTLE (71335-0070-1)Marketed from Mar 15, 2018
71335-0070-27133500700230 TABLET in 1 BOTTLE (71335-0070-2)Marketed from Mar 20, 2018
71335-0070-37133500700320 TABLET in 1 BOTTLE (71335-0070-3)Marketed from Mar 30, 2018
71335-0070-47133500700460 TABLET in 1 BOTTLE (71335-0070-4)Marketed from Aug 8, 2019
71335-0070-5713350070056 TABLET in 1 BOTTLE (71335-0070-5)Marketed from Mar 28, 2018
71335-0070-67133500700610 TABLET in 1 BOTTLE (71335-0070-6)Marketed from Feb 28, 2018
71335-0070-77133500700728 TABLET in 1 BOTTLE (71335-0070-7)Marketed from Jun 4, 2018
71335-0070-871335007008100 TABLET in 1 BOTTLE (71335-0070-8)Marketed from May 4, 2018
71335-0070-97133500700940 TABLET in 1 BOTTLE (71335-0070-9)Marketed from Jun 28, 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)
ciprofloxacin
Generic name (nonproprietary)
ciprofloxacin
Active ingredients
Ciprofloxacin hydrochloride — 500 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076639
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 1A2 Inhibitors (Mechanism)Fluoroquinolones (Chemical structure)
Identifiers
Product ID 71335-0070_7e450b73-3a77-48fb-8552-4d85d44f966fSPL ID 7e450b73-3a77-48fb-8552-4d85d44f966fSPL set ID a5ecc693-b8fd-4a7a-8040-e56f801c9353RxCUI 309309UNII 4BA73M5E37

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

N471335007000 followed by a unit qualifier and the quantity

Package 71335-0070-00. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 076639

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

FDA NDC Directory listings under ANDA 076639
ProductStrengthForm · routeLabelerProduct NDC
ciprofloxacinCiprofloxacin hydrochloride 500 mg/1TabletOralNuCare Pharmaceuticals, Inc.66267-716
ciprofloxacinCiprofloxacin hydrochloride 750 mg/1TabletOralProficient Rx LP63187-990
ciprofloxacinCiprofloxacin hydrochloride 500 mg/1TabletOralNuCare Pharmaceuticals, Inc.66267-919
ciprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralQPharma, Inc.42708-192
ciprofloxacinCiprofloxacin hydrochloride 500 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-869
ciprofloxacinCiprofloxacin hydrochloride 250 mg/1TabletOralBryant Ranch Prepack71335-0408
ciprofloxacinCiprofloxacin hydrochloride 750 mg/1TabletOralCoupler LLC67046-1528
ciprofloxacinCiprofloxacin hydrochloride 750 mg/1Tablet, Film coatedOralRising Pharma Holdings, Inc.16571-413
ciprofloxacinCiprofloxacin hydrochloride 250 mg/1TabletOralPharmPak, Inc.54348-662
ciprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralRising Pharma Holdings, Inc.16571-411
ciprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralRising Pharma Holdings, Inc.16571-412
ciprofloxacinCiprofloxacin hydrochloride 500 mg/1TabletOralPharmPak, Inc.54348-663
ciprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-0193
ciprofloxacinCiprofloxacin hydrochloride 250 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-410
ciprofloxacinCiprofloxacin hydrochloride 500 mg/1TabletOralUmasuto, LLC85293-003
ciprofloxacinCiprofloxacin hydrochloride 250 mg/1TabletOralUmasuto, LLC85293-002
ciprofloxacinCiprofloxacin hydrochloride 750 mg/1TabletOralUmasuto, LLC85293-004
ciprofloxacinCiprofloxacin hydrochloride 500 mg/1TabletOralProficient Rx LP63187-017
ciprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC82868-102
ciprofloxacinCiprofloxacin hydrochloride 500 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4122

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