Prescription drug · ANDA
Bupropion Hydrochloride NDC 67046-1587
Bupropion hydrochloride 75 mg/1 · Tablet · Oral · Coupler LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 67046-1587-3 | 6704615870367046158703 | 30 TABLET in 1 BLISTER PACK (67046-1587-3)Marketed from Sep 16, 2025 |
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 — 75 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Coupler LLCNDC labeler code 67046
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 206975
- 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 67046-1587_3eec6253-ab66-d5b0-e063-6394a90a522dSPL ID 3eec6253-ab66-d5b0-e063-6394a90a522dSPL set ID 3eec57be-b8ae-cdf8-e063-6394a90a694dRxCUI 993691UNII 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
N467046158703followed by a unit qualifier and the quantityPackage 67046-1587-03. 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 an aminoketone antidepressant, indicated for the treatment of major depressive disorder (MDD). ( 1 ) 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) ].
Excerpt only. Read the full label for complete information.
About NDC 67046-1587
- What is NDC 67046-1587?
- 67046-1587 is the product NDC for Bupropion Hydrochloride, Bupropion hydrochloride 75 mg/1 tablet, 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?
- 171 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.
Related NDCs: other Bupropion Hydrochloride products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Bupropion hydrochloride | Bupropion hydrochloride 300 mg/1 | Tablet, Extended releaseOral | REMEDYREPACK INC. | 70518-4739 | 70518-4739-00 |
| Bupropion Hydrochloride | Bupropion hydrochloride 100 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-1143 | 67046-1143-03 |
| Bupropion Hydrochloride | Bupropion hydrochloride 150 mg/1 | Tablet, Film coated, Extended releaseOral | Aurobindo Pharma Limited | 59651-511 | 59651-0511-0559651-0511-3059651-0511-90 |
| Bupropion Hydrochloride | Bupropion hydrochloride 300 mg/1 | Tablet, Film coated, Extended releaseOral | Aurobindo Pharma Limited | 59651-512 | 59651-0512-0559651-0512-3059651-0512-90 |
| Bupropion hydrochloride | Bupropion hydrochloride 150 mg/1 | Tablet, Extended releaseOral | Coupler LLC | 67046-1273 | 67046-1273-03 |
| Bupropion hydrochloride | Bupropion hydrochloride 300 mg/1 | TabletOral | Unit Dose Solutions, Inc. | 87441-014 | 87441-0014-01 |
| bupropion hydrochloride | Bupropion hydrochloride 150 mg/1 | Tablet, Extended releaseOral | REMEDYREPACK INC. | 70518-4674 | 70518-4674-0070518-4674-0170518-4674-02 |
| Bupropion Hydrochloride | Bupropion hydrochloride 75 mg/1 | Tablet, Film coatedOral | Amici Pharma, Inc. | 69292-601 | 69292-0601-01 |
| Bupropion Hydrochloride | Bupropion hydrochloride 100 mg/1 | Tablet, Film coatedOral | Amici Pharma, Inc. | 69292-602 | 69292-0602-01 |
| bupropion Hydrochloride | Bupropion hydrochloride 100 mg/1 | TabletOral | Coupler LLC | 67046-1672 | 67046-1672-03 |
Other NDCs under ANDA 206975
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| bupropion Hydrochloride | Bupropion hydrochloride 100 mg/1 | TabletOral | Coupler LLC | 67046-1672 |
| bupropion Hydrochloride | Bupropion hydrochloride 100 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 43063-994 |
| bupropion Hydrochloride | Bupropion hydrochloride 75 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-0791 |
| Bupropion Hydrochloride | Bupropion hydrochloride 75 mg/1 | TabletOral | MAJOR PHARMACEUTICALS | 0904-7529 |
| bupropion Hydrochloride | Bupropion hydrochloride 75 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-2400 |
| bupropion Hydrochloride | Bupropion hydrochloride 100 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-2401 |
| Bupropion Hydrochloride | Bupropion hydrochloride 100 mg/1 | TabletOral | MAJOR PHARMACEUTICALS | 0904-7530 |
| bupropion Hydrochloride | Bupropion hydrochloride 75 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-2867 |
| bupropion Hydrochloride | Bupropion hydrochloride 100 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-2875 |
| bupropion Hydrochloride | Bupropion hydrochloride 75 mg/1 | TabletOral | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-191 |
| bupropion Hydrochloride | Bupropion hydrochloride 100 mg/1 | TabletOral | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-192 |
| Bupropion Hydrochloride | Bupropion hydrochloride 100 mg/1 | TabletOral | Coupler LLC | 67046-1562 |
| bupropion Hydrochloride | Bupropion hydrochloride 100 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 72789-544 |
| bupropion Hydrochloride | Bupropion hydrochloride 100 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-2690 |
| bupropion Hydrochloride | Bupropion hydrochloride 75 mg/1 | TabletOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-866 |
| Bupropion Hydrochloride | Bupropion hydrochloride 75 mg/1 | TabletOral | Chartwell RX, LLC | 62135-723 |
| bupropion Hydrochloride | Bupropion hydrochloride 100 mg/1 | TabletOral | Northwind Health Company, LLC | 51655-390 |
| Bupropion Hydrochloride | Bupropion hydrochloride 100 mg/1 | TabletOral | Chartwell RX, LLC | 62135-724 |
| Bupropion Hydrochloride | Bupropion hydrochloride 75 mg/1 | TabletOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-899 |