Prescription drug · ANDA

Bupropion Hydrochloride NDC 67046-1143

Bupropion hydrochloride 100 mg/1 · Tablet, Film coated · Oral · Coupler LLC

NDC codes

FDA NDC Directory
Product NDC (as listed)67046-1143Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67046-1143Add 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
67046-1143-36704611430330 TABLET, FILM COATED in 1 BLISTER PACK (67046-1143-3)Marketed from Aug 3, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 Hydrochloride
Generic name (nonproprietary)
bupropion hydrochloride
Active ingredients
Bupropion hydrochloride — 100 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Coupler LLCNDC labeler code 67046
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076143
Marketing start
Listing expires
Other FDA classes
Dopamine Uptake Inhibitors (Mechanism)Increased Dopamine Activity (Physiologic effect)Increased Norepinephrine Activity (Physiologic effect)Norepinephrine Uptake Inhibitors (Mechanism)
Identifiers
Product ID 67046-1143_5829a21b-ff83-686e-e063-6394a90a73ddSPL ID 5829a21b-ff83-686e-e063-6394a90a73ddSPL set ID 5829a2aa-4845-b58b-e063-6294a90ad2f4RxCUI 993687UNII ZG7E5POY8O
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

N467046114303 followed by a unit qualifier and the quantity

Package 67046-1143-03. 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)

Bupropion hydrochloride tablets are indicated for the treatment of major depressive disorder (MDD), as defined by the Diagnostic and Statistical Manual (DSM). The efficacy of bupropion hydrochloride tablets in the treatment of a major depressive episode was established in two 4-week controlled inpatient trials and one 6-week controlled outpatient trial of adult subjects with MDD [see Clinical Studies ( 14 )]. Bupropion hydrochloride tablets are an aminoketone antidepressant, indicated for the treatment of major depressive disorder (MDD). ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 67046-1143

What is NDC 67046-1143?
67046-1143 is the product NDC for Bupropion Hydrochloride, Bupropion hydrochloride 100 mg/1 tablet, film coated, listed with the FDA by Coupler LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Bupropion Hydrochloride.
What is the active ingredient?
Bupropion hydrochloride.
Who is the labeler?
Coupler LLC, NDC labeler code 67046. 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 Hydrochloride?
177 other product NDCs are listed under this name. See all Bupropion 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 Bupropion Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Bupropion hydrochlorideBupropion hydrochloride 300 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-473970518-4739-00
Bupropion HydrochlorideBupropion hydrochloride 150 mg/1Tablet, Film coated, Extended releaseOralAurobindo Pharma Limited59651-51159651-0511-0559651-0511-3059651-0511-90
Bupropion HydrochlorideBupropion hydrochloride 300 mg/1Tablet, Film coated, Extended releaseOralAurobindo Pharma Limited59651-51259651-0512-0559651-0512-3059651-0512-90
Bupropion hydrochlorideBupropion hydrochloride 150 mg/1Tablet, Extended releaseOralCoupler LLC67046-127367046-1273-03
Bupropion hydrochlorideBupropion hydrochloride 300 mg/1TabletOralUnit Dose Solutions, Inc.87441-01487441-0014-01
bupropion hydrochlorideBupropion hydrochloride 150 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-467470518-4674-0070518-4674-01
Bupropion HydrochlorideBupropion hydrochloride 75 mg/1Tablet, Film coatedOralAmici Pharma, Inc.69292-60169292-0601-01
Bupropion HydrochlorideBupropion hydrochloride 100 mg/1Tablet, Film coatedOralAmici Pharma, Inc.69292-60269292-0602-01
bupropion HydrochlorideBupropion hydrochloride 100 mg/1TabletOralCoupler LLC67046-167267046-1672-03
Bupropion HydrochlorideBupropion hydrochloride 75 mg/1Tablet, Film coatedOralCoupler LLC67046-087267046-0872-03

All 178 Bupropion Hydrochloride NDCs

Other NDCs under ANDA 076143

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

FDA NDC Directory listings under ANDA 076143
ProductStrengthForm · routeLabelerProduct NDC
Bupropion HCLBupropion hydrochloride 100 mg/1Tablet, Film coatedOralDirect_Rx72189-457
Bupropion HydrochlorideBupropion hydrochloride 75 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6635
Bupropion HydrochlorideBupropion hydrochloride 100 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6636
Bupropion HydrochlorideBupropion hydrochloride 75 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-880
Bupropion HydrochlorideBupropion hydrochloride 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-1869
Bupropion HydrochlorideBupropion hydrochloride 75 mg/1Tablet, Film coatedOralAvPAK50268-142
Bupropion HydrochlorideBupropion hydrochloride 100 mg/1Tablet, Film coatedOralAvPAK50268-143
Bupropion HydrochlorideBupropion hydrochloride 75 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-4152
Bupropion HydrochlorideBupropion hydrochloride 75 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-8180
Bupropion HydrochlorideBupropion hydrochloride 75 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.60429-746
Bupropion HydrochlorideBupropion hydrochloride 100 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.60429-747
Bupropion HydrochlorideBupropion hydrochloride 100 mg/1Tablet, Film coatedOralApotex Corp60505-0157
Bupropion HydrochlorideBupropion hydrochloride 75 mg/1Tablet, Film coatedOralApotex Corp60505-0158
Bupropion HydrochlorideBupropion hydrochloride 75 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-340
Bupropion HydrochlorideBupropion hydrochloride 100 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-351
Bupropion HydrochlorideBupropion hydrochloride 100 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-781
Bupropion HydrochlorideBupropion hydrochloride 75 mg/1Tablet, Film coatedOralCoupler LLC67046-0872
Bupropion HydrochlorideBupropion hydrochloride 75 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-308
Bupropion HydrochlorideBupropion hydrochloride 100 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-309
Bupropion HydrochlorideBupropion hydrochloride 75 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-2256

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