NDC codes

FDA NDC Directory
Product NDC (as listed)65219-388Labeler and product segments. Claims need a package NDC.
Product NDC at billing width65219-0388Add 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
65219-388-01652190388016521903880125 VIAL, SINGLE-DOSE in 1 CARTON (65219-388-01) / 1 mL in 1 VIAL, SINGLE-DOSE (65219-388-00)Marketed from May 10, 2026

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)
Phenylephrine Hydrochloride
Generic name (nonproprietary)
phenylephrine hydrochloride
Active ingredients
Phenylephrine hydrochloride — 10 mg/mL
Dosage form
Injection
Route
Intravenous
Labeler
Fresenius Kabi USA, LLCNDC labeler code 65219
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 210665
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha1-Agonists (Mechanism)
Identifiers
Product ID 65219-388_b54a0c59-e5e4-4fd7-ba91-c991ce87b148SPL ID b54a0c59-e5e4-4fd7-ba91-c991ce87b148SPL set ID b54a0c59-e5e4-4fd7-ba91-c991ce87b148RxCUI 1666372UNII 04JA59TNSJUPC 0365219388005
Pharmacologic class
alpha-1 Adrenergic Agonist

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

N465219038801 followed by a unit qualifier and the quantity

Package 65219-0388-01. 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)

Phenylephrine Hydrochloride Injection 10 mg/mL is indicated for increasing blood pressure in adults with clinically important hypotension resulting primarily from vasodilation in the settings of anesthesia and septic shock. Phenylephrine Hydrochloride Injection 10 mg/mL is alpha-1 adrenergic receptor agonist indicated for increasing blood pressure in adults with clinically important hypotension resulting primarily from vasodilation in the settings of anesthesia and septic shock.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 65219-388

What is NDC 65219-388?
65219-388 is the product NDC for Phenylephrine Hydrochloride, Phenylephrine hydrochloride 10 mg/mL injection, listed with the FDA by Fresenius Kabi USA, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Phenylephrine Hydrochloride.
What is the active ingredient?
Phenylephrine hydrochloride.
Who is the labeler?
Fresenius Kabi USA, LLC, NDC labeler code 65219. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Phenylephrine Hydrochloride?
107 other product NDCs are listed under this name. See all Phenylephrine Hydrochloride 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 Phenylephrine Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Phenylephrine HydrochloridePhenylephrine hydrochloride 25 mg/mLSolution/ dropsOphthalmicFirst Nation Group, LLC81469-16881469-0168-0281469-0168-15
Phenylephrine HydrochloridePhenylephrine hydrochloride 100 mg/mLSolution/ dropsOphthalmicFirst Nation Group, LLC81469-16981469-0169-05
Phenylephrine HydrochloridePhenylephrine hydrochloride 10 mg/mLInjectionIntravenousCaplin Steriles Limited65145-11565145-0115-25
Phenylephrine HydrochloridePhenylephrine hydrochloride 50 mg/5mLInjectionIntravenousCaplin Steriles Limited65145-11665145-0116-0165145-0116-10
Phenylephrine HydrochloridePhenylephrine hydrochloride 100 mg/10mLInjectionIntravenousCaplin Steriles Limited65145-11765145-0117-01
phenylephrine hydrochloridePhenylephrine hydrochloride 10 mg/mLInjectionIntravenousBaxter Healthcare Corporation36000-35836000-0358-25
phenylephrine hydrochloridePhenylephrine hydrochloride 10 mg/mLInjectionIntravenousBaxter Healthcare Corporation36000-36036000-0360-10
phenylephrine hydrochloridePhenylephrine hydrochloride 10 mg/mLInjectionIntravenousBaxter Healthcare Corporation36000-36236000-0362-05
Phenylephrine HydrochloridePhenylephrine hydrochloride 10 mg/mLInjectionIntravenousMethod Pharmaceuticals, LLC58657-85158657-0851-26
Phenylephrine HydrochloridePhenylephrine hydrochloride 10 mg/mLInjectionIntravenousMethod Pharmaceuticals, LLC58657-85258657-0852-11

All 108 Phenylephrine Hydrochloride NDCs

Other NDCs under ANDA 210665

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

FDA NDC Directory listings under ANDA 210665
ProductStrengthForm · routeLabelerProduct NDC
Phenylephrine HydrochloridePhenylephrine hydrochloride 10 mg/mLInjectionIntravenousHF Acquisition Co LLC, DBA HealthFirst51662-1576
Phenylephrine HydrochloridePhenylephrine hydrochloride 10 mg/mLInjectionIntravenousFresenius Kabi USA, LLC63323-751

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