What is NDC 43063-849?

43063-849 is the product NDC for Furosemide, Furosemide 20 mg/1 tablet, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.

PD-Rx Pharmaceuticals, Inc., NDC labeler code 43063. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Furosemide?

204 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Furosemide NDC 43063-849 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43063-849Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43063-0849Add 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
43063-849-21	4306308492143063084921	21 TABLET in 1 BOTTLE, PLASTIC (43063-849-21)Marketed from Apr 27, 2018
43063-849-30	4306308493043063084930	30 TABLET in 1 BOTTLE, PLASTIC (43063-849-30)Marketed from Apr 27, 2018
43063-849-60	4306308496043063084960	60 TABLET in 1 BOTTLE, PLASTIC (43063-849-60)Marketed from May 3, 2018
43063-849-90	4306308499043063084990	90 TABLET in 1 BOTTLE, PLASTIC (43063-849-90)Marketed from May 3, 2018

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): Furosemide
Generic name (nonproprietary): furosemide
Active ingredients: Furosemide — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: PD-Rx Pharmaceuticals, Inc.NDC labeler code 43063
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076796
Marketing start: Mar 26, 2004
Listing expires: Dec 31, 2026
Other FDA classes: Increased Diuresis at Loop of Henle (Physiologic effect)
Identifiers: Product ID 43063-849_39fd20b5-22d0-8252-e063-6294a90adaadSPL ID 39fd20b5-22d0-8252-e063-6294a90adaadSPL set ID 3ba730ab-90d4-478a-80b3-1ea3edb03e4dRxCUI 310429UNII 7LXU5N7ZO5UPC 0343063849217
Pharmacologic class: Loop Diuretic

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

N443063084921 followed by a unit qualifier and the quantity

Package 43063-0849-21. 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 Jul 15, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Edema Furosemide tablets are indicated in adults and pediatric patients for the treatment of edema associated with congestive heart failure, cirrhosis of the liver, and renal disease, including the nephrotic syndrome. Furosemide tablets are particularly useful when an agent with greater diuretic potential is desired. Hypertension Oral furosemide may be used in adults for the treatment of hypertension alone or in combination with other antihypertensive agents. Hypertensive patients who cannot be adequately controlled with thiazides will probably also not be adequately controlled with furosemide alone.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43063-849

What is NDC 43063-849?: 43063-849 is the product NDC for Furosemide, Furosemide 20 mg/1 tablet, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Furosemide.
What is the active ingredient?: Furosemide.
Who is the labeler?: PD-Rx Pharmaceuticals, Inc., NDC labeler code 43063. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Furosemide?: 204 other product NDCs are listed under this name. See all Furosemide 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 Furosemide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Furosemide	Furosemide 10 mg/mL	InjectionIntramuscular, Intravenous	Civica, Inc.	72572-275	72572-0275-10
Furosemide	Furosemide 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4679	70518-4679-00
Furosemide	Furosemide 20 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-033	87441-0033-01
Furosemide	Furosemide 20 mg/1	TabletOral	Coupler LLC	67046-0768	67046-0768-03
Furosemide	Furosemide 40 mg/1	TabletOral	REMEDYREPACK INC.	70518-4609	70518-4609-00
Furosemide	Furosemide 40 mg/1	TabletOral	Coupler LLC	67046-1663	67046-1663-03
Furosemide	Furosemide 20 mg/1	TabletOral	Marlex Pharmaceuticals, Inc.	10135-832	10135-0832-0110135-0832-1010135-0832-90
Furosemide	Furosemide 40 mg/1	TabletOral	Marlex Pharmaceuticals, Inc.	10135-833	10135-0833-0110135-0833-1010135-0833-90
Furosemide	Furosemide 80 mg/1	TabletOral	Marlex Pharmaceuticals, Inc.	10135-834	10135-0834-0110135-0834-0510135-0834-90
Furosemide	Furosemide 20 mg/1	TabletOral	Granulation Technology, Inc.	63561-0164	63561-0164-0163561-0164-0263561-0164-09

All 205 Furosemide NDCs

Other NDCs under ANDA 076796

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

FDA NDC Directory listings under ANDA 076796
Product	Strength	Form · route	Labeler	Product NDC
Furosemide	Furosemide 40 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-157
Furosemide	Furosemide 40 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4445
Furosemide	Furosemide 40 mg/1	TabletOral	Bryant Ranch Prepack	71335-0842
Furosemide	Furosemide 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-3061
Furosemide	Furosemide 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-0852
Furosemide	Furosemide 80 mg/1	TabletOral	Bryant Ranch Prepack	63629-1119
Furosemide	Furosemide 80 mg/1	TabletOral	Bryant Ranch Prepack	63629-1120
Furosemide	Furosemide 40 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4522
Furosemide	Furosemide 20 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4534
Furosemide	Furosemide 20 mg/1	TabletOral	Bryant Ranch Prepack	63629-1214
Furosemide	Furosemide 20 mg/1	TabletOral	Bryant Ranch Prepack	63629-1215
Furosemide	Furosemide 40 mg/1	TabletOral	Bryant Ranch Prepack	63629-1216
Furosemide	Furosemide 40 mg/1	TabletOral	Bryant Ranch Prepack	63629-1217
Furosemide	Furosemide 20 mg/1	TabletOral	Bryant Ranch Prepack	72162-1360
Furosemide	Furosemide 40 mg/1	TabletOral	Bryant Ranch Prepack	72162-1361
Furosemide	Furosemide 80 mg/1	TabletOral	Bryant Ranch Prepack	72162-1362
Furosemide	Furosemide 20 mg/1	TabletOral	Major Pharmaceuticals	0904-7177
Furosemide	Furosemide 40 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-049
Furosemide	Furosemide 20 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8368
Furosemide	Furosemide 40 mg/1	TabletOral	Major Pharmaceuticals	0904-7178

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