What is NDC 71205-922?

71205-922 is the product NDC for Felodipine, Felodipine 10 mg/1 tablet, film coated, listed with the FDA by Proficient Rx LP. It has 6 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Felodipine?

49 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Felodipine NDC 71205-922 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-922Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0922Add 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
71205-922-00	7120509220071205092200	100 TABLET, FILM COATED in 1 BOTTLE (71205-922-00)Marketed from Jun 18, 2021
71205-922-30	7120509223071205092230	30 TABLET, FILM COATED in 1 BOTTLE (71205-922-30)Marketed from Jun 18, 2021
71205-922-55	7120509225571205092255	500 TABLET, FILM COATED in 1 BOTTLE (71205-922-55)Marketed from Jun 18, 2021
71205-922-60	7120509226071205092260	60 TABLET, FILM COATED in 1 BOTTLE (71205-922-60)Marketed from Jun 18, 2021
71205-922-72	7120509227271205092272	120 TABLET, FILM COATED in 1 BOTTLE (71205-922-72)Marketed from Jun 18, 2021
71205-922-90	7120509229071205092290	90 TABLET, FILM COATED in 1 BOTTLE (71205-922-90)Marketed from Jun 18, 2021

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): Felodipine
Generic name (nonproprietary): felodipine
Active ingredients: Felodipine — 10 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 71205
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204800
Marketing start: Oct 12, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Calcium Channel Antagonists (Mechanism)Dihydropyridines (Chemical structure)
Identifiers: Product ID 71205-922_06c9bc5a-7a0f-483d-bd5c-61768db340bbSPL ID 06c9bc5a-7a0f-483d-bd5c-61768db340bbSPL set ID 2c4dd9a4-61ca-4c88-90f6-12d9e0fdb7cdRxCUI 402695, 402696, 402698UNII OL961R6O2CUPC 0371205920302
Pharmacologic class: Dihydropyridine Calcium Channel 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 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

N471205092200 followed by a unit qualifier and the quantity

Package 71205-0922-00. 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 Apr 1, 2022.

Indications (excerpt from the label)

INDICATIONS AND USAGE Felodipine extended-release tablets, USP are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure lowers the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including felodipine. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise and limited sodium intake. Many patients will require more than one drug to ac…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-922

What is NDC 71205-922?: 71205-922 is the product NDC for Felodipine, Felodipine 10 mg/1 tablet, film coated, listed with the FDA by Proficient Rx LP. It has 6 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Felodipine.
What is the active ingredient?: Felodipine.
Who is the labeler?: Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Felodipine?: 49 other product NDCs are listed under this name. See all Felodipine 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 Felodipine NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Felodipine	Felodipine 2.5 mg/1	Tablet, Extended releaseOral	Westminster Pharmaceuticals, LLC	69367-264	69367-0264-01
Felodipine	Felodipine 5 mg/1	Tablet, Extended releaseOral	Westminster Pharmaceuticals, LLC	69367-265	69367-0265-01
Felodipine	Felodipine 2.5 mg/1	Tablet, Film coatedOral	Carlsbad Technology, Inc.	61442-431	61442-0431-0161442-0431-05
Felodipine	Felodipine 5 mg/1	Tablet, Film coatedOral	Carlsbad Technology, Inc.	61442-432	61442-0432-0161442-0432-05
Felodipine	Felodipine 10 mg/1	Tablet, Film coatedOral	Carlsbad Technology, Inc.	61442-433	61442-0433-0161442-0433-05
Felodipine	Felodipine 10 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-2016	63629-2016-01
Felodipine	Felodipine 2.5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-2017	63629-2017-01
Felodipine	Felodipine 5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-2018	63629-2018-01
Felodipine	Felodipine 2.5 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-920	71205-0920-0071205-0920-3071205-0920-55+3 more
Felodipine	Felodipine 5 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-921	71205-0921-0071205-0921-3071205-0921-55+3 more

All 50 Felodipine NDCs

Other NDCs under ANDA 204800

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

FDA NDC Directory listings under ANDA 204800
Product	Strength	Form · route	Labeler	Product NDC
Felodipine	Felodipine 5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2175
Felodipine	Felodipine 2.5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-2017
Felodipine	Felodipine 10 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-2016
Felodipine	Felodipine 5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-2018
Felodipine	Felodipine 5 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-088
Felodipine	Felodipine 10 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-089
Felodipine	Felodipine 2.5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-1742
Felodipine	Felodipine 5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-1743
Felodipine	Felodipine 10 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-1744
Felodipine	Felodipine 10 mg/1	Tablet, Film coatedOral	Carlsbad Technology, Inc.	61442-433
Felodipine	Felodipine 2.5 mg/1	Tablet, Film coatedOral	Carlsbad Technology, Inc.	61442-431
Felodipine	Felodipine 5 mg/1	Tablet, Film coatedOral	Carlsbad Technology, Inc.	61442-432
Felodipine	Felodipine 2.5 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-920
Felodipine	Felodipine 5 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-921