Ampicillin (ampicillin sodium) NDC 65219-014

NDC codes

FDA NDC Directory

Product NDC (as listed)65219-014Labeler and product segments. Claims need a package NDC.

Product NDC at billing width65219-0014Add 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
65219-014-10	65219001410	10 VIAL in 1 CARTON (65219-014-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (65219-014-01)Marketed from Oct 30, 2019

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): Ampicillin
Generic name (nonproprietary): ampicillin sodium
Active ingredients: Ampicillin sodium — 250 mg/1
Dosage form: Injection, Powder, For solution
Route: Intramuscular, Intravenous
Labeler: Fresenius Kabi USA, LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 062719
Marketing start: Oct 30, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Penicillins (Chemical structure)
Identifiers: Product ID 65219-014_38c6c088-e4ab-4859-b4d9-89e846cf9d5fSPL ID 38c6c088-e4ab-4859-b4d9-89e846cf9d5fSPL set ID 8dbb4c71-8543-08f1-e053-2995a90af88dRxCUI 1721473, 1721474, 1721475, 1721476UNII JFN36L5S8K
Pharmacologic class: Penicillin-class Antibacterial

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N465219001410 followed by a unit qualifier and the quantity

Package 65219-0014-10. 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

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

Other NDCs under ANDA 062719

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

FDA NDC Directory listings under ANDA 062719
Product	Strength	Form · route	Labeler	Product NDC
Ampicillinampicillin sodium	Ampicillin sodium 1 g/1	Injection, Powder, For solutionIntramuscular, Intravenous	NorthStar Rx, LLC	72603-363
Ampicillin	Ampicillin sodium 250 mg/1	Injection, Powder, For solutionIntramuscular, Intravenous	HF Acquisition Co LLC, DBA HealthFirst	51662-1595
Ampicillin	Ampicillin sodium 1 g/1	Injection, Powder, For solutionIntramuscular, Intravenous	Civica, Inc.	72572-016
Ampicillinampicillin sodium	Ampicillin sodium 500 mg/1	Injection, Powder, For solutionIntramuscular, Intravenous	NorthStar Rx, LLC	72603-221
Ampicillinampicillin sodium	Ampicillin sodium 500 mg/1	Injection, Powder, For solutionIntramuscular, Intravenous	Fresenius Kabi USA, LLC	65219-016
Ampicillinampicillin sodium	Ampicillin sodium 1 g/1	Injection, Powder, For solutionIntramuscular, Intravenous	Fresenius Kabi USA, LLC	65219-018