NDC codes

FDA NDC Directory
Product NDC (as listed)70518-2607Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-2607Add 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
70518-2607-1705182607017051826070128 CAPSULE in 1 BOTTLE, PLASTIC (70518-2607-1)Marketed from Jul 17, 2025

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)
Ampicillin
Generic name (nonproprietary)
ampicillin
Active ingredients
Ampicillin trihydrate — 500 mg/1
Dosage form
Capsule
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 064082
Marketing start
Listing expires
Other FDA classes
Penicillins (Chemical structure)
Identifiers
Product ID 70518-2607_579aef6a-084d-183b-e063-6394a90ae137SPL ID 579aef6a-084d-183b-e063-6394a90ae137SPL set ID 4134cd79-c895-4e6e-b1d5-8e01c38bf2d1RxCUI 308212UNII HXQ6A1N7R6

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

N470518260701 followed by a unit qualifier and the quantity

Package 70518-2607-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE To reduce the development of drug-resistant bacteria and maintain the effectiveness of ampicillin capsules, ampicillin for oral suspension and other antibacterial drugs, ampicillin capsules and ampicillin for oral suspension should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. When culture and susceptibility information are available, they should be considered in selecting of modifying antimicrobial therapy, in the absence of such data, local epidemiology and susceptibility patterns contribute to the empiric selection of therapy. Ampicillin capsules and ampicillin for oral suspension are indicated in the trea…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-2607

What is NDC 70518-2607?
70518-2607 is the product NDC for Ampicillin, Ampicillin trihydrate 500 mg/1 capsule, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ampicillin.
What is the active ingredient?
Ampicillin trihydrate.
Who is the labeler?
REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ampicillin?
68 other product NDCs are listed under this name. See all Ampicillin 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 Ampicillin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Ampicillinampicillin sodiumAmpicillin sodium 1 g/1Injection, Powder, For solutionIntramuscular, IntravenousHenry Schein, Inc.0404-976000404-9760-99
AmpicillinAmpicillin sodium 500 mg/1Injection, Powder, For solutionIntramuscular, IntravenousONESOURCE SPECIALTY PHARMA LIMITED83270-31283270-0312-10
AmpicillinAmpicillin sodium 250 mg/1Injection, Powder, For solutionIntramuscular, IntravenousONESOURCE SPECIALTY PHARMA LIMITED83270-31183270-0311-10
AmpicillinAmpicillin sodium 1 g/1Injection, Powder, For solutionIntramuscular, IntravenousONESOURCE SPECIALTY PHARMA LIMITED83270-31383270-0313-10
AmpicillinAmpicillin sodium 2 g/1Injection, Powder, For solutionIntravenousONESOURCE SPECIALTY PHARMA LIMITED83270-31483270-0314-10
AmpicillinAmpicillin sodium 10 g/1Injection, Powder, For solutionIntravenousONESOURCE SPECIALTY PHARMA LIMITED83270-31583270-0315-01
AmpicillinAmpicillin sodium 10 g/1Injection, Powder, For solutionIntravenousArmas Pharmaceuticals Inc.72485-42372485-0423-10
Ampicillinampicillin sodiumAmpicillin sodium 10 g/100mLInjection, Powder, For solutionIntravenousAvenacy Inc.83634-10083634-0100-99
Ampicillinampicillin injectionAmpicillin sodium 500 mg/500mgPowder, For solutionIntramuscular, IntravenousHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-91523155-0915-41
Ampicillinampicillin injectionAmpicillin sodium 250 mg/250mgPowder, For solutionIntramuscular, IntravenousHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-91423155-0914-41

All 69 Ampicillin NDCs

Other NDCs under ANDA 064082

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

FDA NDC Directory listings under ANDA 064082
ProductStrengthForm · routeLabelerProduct NDC
AmpicillinAmpicillin trihydrate 500 mg/1CapsuleOralSandoz Inc0781-2145

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