What is NDC 71872-7096?

71872-7096 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 1 mg/mL injection, listed with the FDA by Medical Purchasing Solutions, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Medical Purchasing Solutions, LLC, NDC labeler code 71872. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Propranolol Hydrochloride?

196 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Propranolol Hydrochloride NDC 71872-7096

NDC codes

FDA NDC Directory

Product NDC (as listed)71872-7096Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71872-7096Add 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
71872-7096-1	71872709601	1 VIAL in 1 BAG (71872-7096-1) / 1 mL in 1 VIALMarketed from Mar 30, 2018

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): Propranolol Hydrochloride
Generic name (nonproprietary): propranolol hydrochloride
Active ingredients: Propranolol hydrochloride — 1 mg/mL
Dosage form: Injection
Route: Intravenous
Labeler: Medical Purchasing Solutions, LLCNDC labeler code 71872
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077760
Marketing start: Jan 31, 2008
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 71872-7096_fc5e5df1-f935-b388-e053-6394a90a37abSPL ID fc5e5df1-f935-b388-e053-6394a90a37abSPL set ID 693569bd-6053-5b3e-e053-2a91aa0a6e9cRxCUI 856443UNII F8A3652H1V
Pharmacologic class: beta-Adrenergic Blocker

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

N471872709601 followed by a unit qualifier and the quantity

Package 71872-7096-01. 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 May 23, 2023.

Indications (excerpt from the label)

INDICATIONS AND USAGE Cardiac Arrhythmias Intravenous administration is usually reserved for life-threatening arrhythmias or those occurring under anesthesia. 1. Supraventricular arrhythmias Intravenous propranolol is indicated for the short-term treatment of supraventricular tachycardia, including Wolff‑Parkinson‑White syndrome and thyrotoxicosis, to decrease ventricular rate. Use in patients with atrial flutter or atrial fibrillation should be reserved for arrythmias unresponsive to standard therapy or when more prolonged control is required. Reversion to normal sinus rhythm has occasionally been observed, predominantly in patients with sinus or atrial tachycardia. 2. Ventricular tachycard…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71872-7096

What is NDC 71872-7096?: 71872-7096 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 1 mg/mL injection, listed with the FDA by Medical Purchasing Solutions, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Propranolol Hydrochloride.
What is the active ingredient?: Propranolol hydrochloride.
Who is the labeler?: Medical Purchasing Solutions, LLC, NDC labeler code 71872. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Propranolol Hydrochloride?: 196 other product NDCs are listed under this name. See all Propranolol 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 Propranolol Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Propranolol Hydrochloride	Propranolol hydrochloride 40 mg/1	TabletOral	American Health Packaging	60687-948	60687-0948-01
Propranolol Hydrochloride	Propranolol hydrochloride 60 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-132	82619-0132-0182619-0132-02
Propranolol Hydrochloride	Propranolol hydrochloride 80 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-133	82619-0133-0182619-0133-02
Propranolol Hydrochloride	Propranolol hydrochloride 120 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-134	82619-0134-0182619-0134-02
Propranolol Hydrochloride	Propranolol hydrochloride 160 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-135	82619-0135-0182619-0135-02
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-4958	00121-4958-40
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-0958	00121-0958-16
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2584	55154-2584-00
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	American Health Packaging	60687-937	60687-0937-01
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0583	80425-0583-0180425-0583-0280425-0583-03

All 197 Propranolol Hydrochloride NDCs

Other NDCs under ANDA 077760

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

FDA NDC Directory listings under ANDA 077760
Product	Strength	Form · route	Labeler	Product NDC
Propranolol Hydrochloride	Propranolol hydrochloride 1 mg/mL	InjectionIntravenous	HF Acquisition Co LLC, DBA HealthFirst	51662-1338
Propranolol Hydrochloride	Propranolol hydrochloride 1 mg/mL	InjectionIntravenous	Hikma Pharmaceuticals USA Inc.	0143-9872