NDC codes

FDA NDC Directory
Product NDC (as listed)68071-1675Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-1675Add 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
68071-1675-168071167501100 mL in 1 BOTTLE (68071-1675-1)Marketed from Sep 20, 2017

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)
Amoxicillin
Generic name (nonproprietary)
amoxicillin
Active ingredients
Amoxicillin — 400 mg/5mL
Dosage form
Powder, For suspension
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 065325
Marketing start
Listing expires
Other FDA classes
Penicillins (Chemical structure)
Identifiers
Product ID 68071-1675_2a31a975-72fc-2a16-e063-6394a90a8149SPL ID 2a31a975-72fc-2a16-e063-6394a90a8149SPL set ID 59a546ed-84b7-a54a-e053-2991aa0a3a0dRxCUI 308189UNII 804826J2HUUPC 0368071167511

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

N468071167501 followed by a unit qualifier and the quantity

Package 68071-1675-01. 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)

To reduce the development of drug-resistant bacteria and maintain the effectiveness of Amoxicillin and other antibacterial drugs, Amoxicillin for Oral Suspension, USP should be used only to treat 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 or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Amoxicillin for Oral Suspension, USP is indicated in the treatment of infections due to susceptible (ONLY β-lactamase–negative) isolates of the designated bacteria in …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 065325

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

FDA NDC Directory listings under ANDA 065325
ProductStrengthForm · routeLabelerProduct NDC
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralHikma Pharmaceuticals USA Inc.0143-9887
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralPreferred Pharmaceuticals Inc.68788-8730
Amoxilamoxicillin oral suspAmoxicillin 400 mg/5mLPowder, For suspensionOralDirectRx72189-385
AmoxicillinAmoxicillin 200 mg/5mLPowder, For suspensionOralPreferred Pharmaceuticals Inc.68788-7323
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralA-S Medication Solutions50090-0858
AmoxicillinAmoxicillin 200 mg/5mLPowder, For suspensionOralPreferred Pharmaceuticals Inc.68788-8852
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralProficient Rx LP71205-422
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralNuCare Pharmaceuticals,Inc.68071-4796
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralA-S Medication Solutions50090-1086
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralA-S Medication Solutions50090-1347
AmoxicillinAmoxicillin 200 mg/5mLPowder, For suspensionOralHikma Pharmaceuticals USA Inc.0143-9886

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