NDC codes

FDA NDC Directory
Product NDC (as listed)69680-130Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69680-0130Add 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
69680-130-60696800130606968001306060 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69680-130-60)Marketed from Jan 28, 2019
69680-130-926968001309269680013092500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69680-130-92)Marketed from Jan 28, 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)
Propafenone Hydrochloride
Generic name (nonproprietary)
propafenone
Active ingredients
Propafenone hydrochloride — 225 mg/1
Dosage form
Capsule, Extended release
Route
Oral
Labeler
Vitruvias TherapeuticsNDC labeler code 69680
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 210339
Marketing start
Listing expires
Identifiers
Product ID 69680-130_827a5fb5-9318-4116-9e23-6b75e469dd77SPL ID 827a5fb5-9318-4116-9e23-6b75e469dd77SPL set ID bc1d2548-15a3-4986-92b1-c3ddfb35343aRxCUI 861156, 861164, 861171UNII 33XCH0HOCDUPC 0369680132600, 0369680130606, 0369680130927, 0369680132921, 0369680131924, 0369680131603
Pharmacologic class
Antiarrhythmic

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

N469680013060 followed by a unit qualifier and the quantity

Package 69680-0130-60. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Propafenone hydrochloride extended-release capsules is indicated to prolong the time to recurrence of symptomatic atrial fibrillation (AF) in patients with episodic (most likely paroxysmal or persistent) AF who do not have structural heart disease. Usage Considerations: The use of propafenone hydrochloride extended-release capsules in patients with permanent AF or in patients exclusively with atrial flutter or paroxysmal supraventricular tachycardia (PSVT) has not been evaluated. Do not use propafenone hydrochloride extended-release capsules to control ventricular rate during AF. Some patients with atrial flutter treated with propafenone have developed 1:1 conduction, producing an increase i…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69680-130

What is NDC 69680-130?
69680-130 is the product NDC for Propafenone Hydrochloride (propafenone), Propafenone hydrochloride 225 mg/1 capsule, extended release, listed with the FDA by Vitruvias Therapeutics. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Propafenone Hydrochloride (Propafenone).
What is the active ingredient?
Propafenone hydrochloride.
Who is the labeler?
Vitruvias Therapeutics, NDC labeler code 69680. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Propafenone Hydrochloride?
52 other product NDCs are listed under this name. See all Propafenone 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 Propafenone Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Propafenone HydrochloridePropafenone hydrochloride 150 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-93060687-0930-01
Propafenone HydrochloridePropafenone hydrochloride 300 mg/1Tablet, Film coatedOralStrides Pharma Science Limited64380-24664380-0246-01
Propafenone HydrochloridePropafenone hydrochloride 225 mg/1Tablet, Film coatedOralStrides Pharma Science Limited64380-26864380-0268-0164380-0268-02
Propafenone HydrochloridePropafenone hydrochloride 150 mg/1Tablet, Film coatedOralStrides Pharma Science Limited64380-26964380-0269-0164380-0269-02
Propafenone HydrochloridePropafenone hydrochloride 225 mg/1Capsule, Extended releaseOralAurobindo Pharma Limited59651-27659651-0276-0559651-0276-6059651-0276-90
Propafenone HydrochloridePropafenone hydrochloride 325 mg/1Capsule, Extended releaseOralAurobindo Pharma Limited59651-27759651-0277-0559651-0277-6059651-0277-90
Propafenone HydrochloridePropafenone hydrochloride 425 mg/1Capsule, Extended releaseOralAurobindo Pharma Limited59651-27859651-0278-0559651-0278-6059651-0278-90
Propafenone HydrochloridePropafenone hydrochloride 150 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-70960687-0709-01
Propafenone HydrochloridePropafenone hydrochloride 300 mg/1Tablet, Film coatedOralStrides Pharma Science Limited64380-16364380-0163-01
Propafenone HydrochloridePropafenone hydrochloride 225 mg/1Tablet, Film coatedOralStrides Pharma Science Limited64380-16464380-0164-0164380-0164-02

All 53 Propafenone Hydrochloride NDCs

Other NDCs under ANDA 210339

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

FDA NDC Directory listings under ANDA 210339
ProductStrengthForm · routeLabelerProduct NDC
Propafenone HydrochloridepropafenonePropafenone hydrochloride 325 mg/1Capsule, Extended releaseOralVitruvias Therapeutics69680-131
Propafenone HydrochloridepropafenonePropafenone hydrochloride 425 mg/1Capsule, Extended releaseOralVitruvias Therapeutics69680-132

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