What is NDC 61919-558?

61919-558 is the product NDC for Bupropion HCL ER (XL), Bupropion hydrochloride 150 mg/1 tablet, extended release, listed with the FDA by Direct_Rx. It has 4 package NDCs, shown above in 10- and 11-digit form.

Direct_Rx, NDC labeler code 61919. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Bupropion HCL ER (XL)?

2 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Bupropion HCL ER (XL) NDC 61919-558

NDC codes

FDA NDC Directory

Product NDC (as listed)61919-558Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61919-0558Add 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
61919-558-30	6191905583061919055830	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-558-30)Marketed from Feb 15, 2024
61919-558-60	6191905586061919055860	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-558-60)Marketed from Feb 15, 2024
61919-558-72	6191905587261919055872	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-558-72)Marketed from Feb 15, 2024
61919-558-90	6191905589061919055890	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-558-90)Marketed from Feb 15, 2024

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): Bupropion HCL ER (XL)
Generic name (nonproprietary): bupropion hcl er (xl)
Active ingredients: Bupropion hydrochloride — 150 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: Direct_RxNDC labeler code 61919
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090693
Marketing start: Feb 15, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Dopamine Uptake Inhibitors (Mechanism)Increased Dopamine Activity (Physiologic effect)Increased Norepinephrine Activity (Physiologic effect)Norepinephrine Uptake Inhibitors (Mechanism)
Identifiers: Product ID 61919-558_5c154150-cdc1-74ed-e063-6294a90ac862SPL ID 5c154150-cdc1-74ed-e063-6294a90ac862
Pharmacologic class: Aminoketone

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

N461919055830 followed by a unit qualifier and the quantity

Package 61919-0558-30. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 61919-558

What is NDC 61919-558?: 61919-558 is the product NDC for Bupropion HCL ER (XL), Bupropion hydrochloride 150 mg/1 tablet, extended release, listed with the FDA by Direct_Rx. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Bupropion HCL ER (XL).
What is the active ingredient?: Bupropion hydrochloride.
Who is the labeler?: Direct_Rx, NDC labeler code 61919. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bupropion HCL ER (XL)?: 2 other product NDCs are listed under this name. See all Bupropion HCL ER (XL) 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 Bupropion HCL ER (XL) NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
BUPROPION HCl ER (XL)bupropion hcl er	Bupropion hydrochloride 450 mg/1	Tablet, Extended releaseOral	Lifestar Pharma LLC	70756-830	70756-0830-1670756-0830-30
Bupropion HCL ER (XL)	Bupropion hydrochloride 300 mg/1	Tablet, Extended releaseOral	Direct_RX	72189-539	72189-0539-3072189-0539-90

Other NDCs under ANDA 090693

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

FDA NDC Directory listings under ANDA 090693
Product	Strength	Form · route	Labeler	Product NDC
Bupropion Hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-4747
Bupropion Hydrochloride	Bupropion hydrochloride 300 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-4749
Bupropion Hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-6789
Bupropion Hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	AvPAK	50268-133
Bupropion Hydrochloride	Bupropion hydrochloride 300 mg/1	Tablet, Extended releaseOral	AvPAK	50268-134
Bupropion Hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	NuCare Pharmaceuticals,Inc.	68071-3559
Bupropion Hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-2022
Bupropion Hydrochloride XLbupropion hydrochloride	Bupropion hydrochloride 300 mg/1	Tablet, Extended releaseOral	Major Pharmaceuticals	0904-7469
Bupropion Hydrochloride XLbupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	Major Pharmaceuticals	0904-7505
Bupropion Hydrochloride XLbupropion hydrochloride	Bupropion hydrochloride 300 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7602
Bupropion Hydrochloride XLbupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	Northwind Health Company, LLC	51655-098
Bupropion Hydrochloride XLbupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	American Health Packaging	60687-782
Bupropion Hydrochloride XLbupropion hydrochloride	Bupropion hydrochloride 300 mg/1	Tablet, Extended releaseOral	American Health Packaging	60687-793
Bupropion Hydrochloride XLbupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-0699
Bupropion Hydrochloride XLbupropion hydrochloride	Bupropion hydrochloride 300 mg/1	Tablet, Extended releaseOral	NuCare Pharmaceuticals,Inc.	68071-3928
Bupropion Hydrochloride XLbupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	NuCare Pharmaceuticals, Inc.	68071-3932
Bupropion Hydrochloride XLbupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	Lupin Pharmaceuticals, Inc.	68180-319
Bupropion Hydrochloride XLbupropion hydrochloride	Bupropion hydrochloride 300 mg/1	Tablet, Extended releaseOral	Lupin Pharmaceuticals, Inc.	68180-320
Bupropion Hydrochloride XLbupropion hydrochloride	Bupropion hydrochloride 300 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4446
Bupropion Hydrochloride XLbupropion hydrochloride	Bupropion hydrochloride 150 mg/1	Tablet, Extended releaseOral	Quallent Pharmaceuticals Health LLC	82009-051

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