NDC codes

FDA NDC Directory
Product NDC (as listed)76420-573Labeler and product segments. Claims need a package NDC.
Product NDC at billing width76420-0573Add 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
76420-573-1076420057310100 mL in 1 BOTTLE (76420-573-10)Marketed from Jun 17, 2023
76420-573-1576420057315150 mL in 1 BOTTLE (76420-573-15)Marketed from Jun 17, 2023
76420-573-807642005738080 mL in 1 BOTTLE (76420-573-80)Marketed from Jun 17, 2023

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)
Amoxicillin
Generic name (nonproprietary)
amoxicillin
Active ingredients
Amoxicillin — 250 mg/5mL
Dosage form
Powder, For suspension
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 061931
Marketing start
Listing expires
Other FDA classes
Penicillins (Chemical structure)
Identifiers
Product ID 76420-573_fe4d14a5-07d5-9345-e053-6294a90a78b2SPL ID fe4d14a5-07d5-9345-e053-6294a90a78b2SPL set ID bfd67724-fb22-4eac-8ebd-555614c16329RxCUI 239191UNII 804826J2HU

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

N476420057310 followed by a unit qualifier and the quantity

Package 76420-0573-10. 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)

Adults and Pediatric Patients Upper Respiratory Tract Infections of the Ear, Nose, and Throat: Amoxicillin for oral suspension are indicated in the treatment of infections due to susceptible (ONLY β-lactamase-negative) isolates of Streptococcus species. (α- and β-hemolytic isolates only), Streptococcus pneumoniae , Staphylococcus spp., or Haemophilus influenzae . Infections of the Genitourinary Tract: Amoxicillin for oral suspension are indicated in the treatment of infections due to susceptible (ONLY β-lactamase-negative) isolates of Escherichia coli , Proteus mirabilis , or Enterococcus faecalis . Infections of the Skin and Skin Structure: Amoxicillin for oral suspension are indicated in t…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 061931

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

FDA NDC Directory listings under ANDA 061931
ProductStrengthForm · routeLabelerProduct NDC
AmoxicillinAmoxicillin 250 mg/5mLPowder, For suspensionOralNuCare Pharmaceuticals,Inc.66267-994
AmoxicillinAmoxicillin 250 mg/5mLPowder, For suspensionOralChartwell RX, LLC62135-089
AmoxicillinAmoxicillin 125 mg/5mLPowder, For suspensionOralChartwell RX, LLC62135-109
AmoxicillinAmoxicillin 250 mg/5mLPowder, For suspensionOralNuCare Pharmaceuticals,Inc.68071-2558
AmoxicillinAmoxicillin 250 mg/5mLPowder, For suspensionOralProficient Rx LP63187-186
AmoxicillinAmoxicillin 250 mg/5mLPowder, For suspensionOralTeva Pharmaceuticals USA, Inc.0093-4155

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