What is NDC 60687-709?

60687-709 is the product NDC for Propafenone Hydrochloride, Propafenone hydrochloride 150 mg/1 tablet, film coated, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.

American Health Packaging, NDC labeler code 60687. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Propafenone Hydrochloride NDC 60687-709

NDC codes

FDA NDC Directory

Product NDC (as listed)60687-709Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60687-0709Add 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
60687-709-01	6068707090160687070901	100 BLISTER PACK in 1 CARTON (60687-709-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-709-11)Marketed from Oct 13, 2022

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 hydrochloride
Active ingredients: Propafenone hydrochloride — 150 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: American Health PackagingNDC labeler code 60687
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075938
Marketing start: Oct 13, 2022
Marketing end: Jan 31, 2027
Identifiers: Product ID 60687-709_3f172eeb-8316-cdbc-e063-6394a90a1e86SPL ID 3f172eeb-8316-cdbc-e063-6394a90a1e86SPL set ID 343e4ad7-05e2-4e6c-8f8e-91c07739cae2RxCUI 861424UNII 33XCH0HOCD
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

N460687070901 followed by a unit qualifier and the quantity

Package 60687-0709-01. 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 Sep 18, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Propafenone hydrochloride tablets are indicated to: prolong the time to recurrence of paroxysmal atrial fibrillation/flutter (PAF) associated with disabling symptoms in patients without structural heart disease. prolong the time to recurrence of paroxysmal supraventricular tachycardia (PSVT) associated with disabling symptoms in patients without structural heart disease. treat documented ventricular arrhythmias, such as sustained ventricular tachycardia that, in the judgment of the physician, are life-threatening. Initiate treatment in the hospital. Usage Considerations: The use of propafenone hydrochloride tablets in patients with permanent atrial fibrillation (AF) or in patients exclusivel…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60687-709

What is NDC 60687-709?: 60687-709 is the product NDC for Propafenone Hydrochloride, Propafenone hydrochloride 150 mg/1 tablet, film coated, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Propafenone Hydrochloride.
What is the active ingredient?: Propafenone hydrochloride.
Who is the labeler?: American Health Packaging, NDC labeler code 60687. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Propafenone Hydrochloride	Propafenone hydrochloride 150 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-930	60687-0930-01
Propafenone Hydrochloride	Propafenone hydrochloride 300 mg/1	Tablet, Film coatedOral	Strides Pharma Science Limited	64380-246	64380-0246-01
Propafenone Hydrochloride	Propafenone hydrochloride 225 mg/1	Tablet, Film coatedOral	Strides Pharma Science Limited	64380-268	64380-0268-0164380-0268-02
Propafenone Hydrochloride	Propafenone hydrochloride 150 mg/1	Tablet, Film coatedOral	Strides Pharma Science Limited	64380-269	64380-0269-0164380-0269-02
Propafenone Hydrochloride	Propafenone hydrochloride 225 mg/1	Capsule, Extended releaseOral	Aurobindo Pharma Limited	59651-276	59651-0276-0559651-0276-6059651-0276-90
Propafenone Hydrochloride	Propafenone hydrochloride 325 mg/1	Capsule, Extended releaseOral	Aurobindo Pharma Limited	59651-277	59651-0277-0559651-0277-6059651-0277-90
Propafenone Hydrochloride	Propafenone hydrochloride 425 mg/1	Capsule, Extended releaseOral	Aurobindo Pharma Limited	59651-278	59651-0278-0559651-0278-6059651-0278-90
Propafenone Hydrochloride	Propafenone hydrochloride 300 mg/1	Tablet, Film coatedOral	Strides Pharma Science Limited	64380-163	64380-0163-01
Propafenone Hydrochloride	Propafenone hydrochloride 225 mg/1	Tablet, Film coatedOral	Strides Pharma Science Limited	64380-164	64380-0164-0164380-0164-02
Propafenone Hydrochloride	Propafenone hydrochloride 150 mg/1	Tablet, Film coatedOral	Strides Pharma Science Limited	64380-165	64380-0165-0164380-0165-02

All 53 Propafenone Hydrochloride NDCs

Other NDCs under ANDA 075938

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

FDA NDC Directory listings under ANDA 075938
Product	Strength	Form · route	Labeler	Product NDC
Propafenone Hydrochloride	Propafenone hydrochloride 150 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-930
Propafenone Hydrochloride	Propafenone hydrochloride 300 mg/1	Tablet, Film coatedOral	Strides Pharma Science Limited	64380-163
Propafenone Hydrochloride	Propafenone hydrochloride 225 mg/1	Tablet, Film coatedOral	Strides Pharma Science Limited	64380-164
Propafenone Hydrochloride	Propafenone hydrochloride 150 mg/1	Tablet, Film coatedOral	Strides Pharma Science Limited	64380-165
Propafenone Hydrochloride	Propafenone hydrochloride 300 mg/1	Tablet, Film coatedOral	Strides Pharma Science Limited	64380-246
Propafenone Hydrochloride	Propafenone hydrochloride 225 mg/1	Tablet, Film coatedOral	Strides Pharma Science Limited	64380-268
Propafenone Hydrochloride	Propafenone hydrochloride 150 mg/1	Tablet, Film coatedOral	Strides Pharma Science Limited	64380-269