NDC 83301-0024-01 - Bupropion Hydrochloride (XL)
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 83301-0024
- Requested NDC
- 83301-0024-01
- Package NDCs from labels
- 83301-0024-1, 83301-0024-2, 83301-0024-3, 83301-0024-4, 83301-0024-01
- Manufacturer
- Mullan Pharmaceutical Inc. | Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd.
- Effective date
- 2026-01-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Bupropion Hydrochloride (XL) | Mullan Pharmaceutical Inc. | Hangzhou Minsheng Binjiang Pharmaceutical Co., Ltd. | 2026-01-29 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83301-0024-1 | Bupropion Hydrochloride (XL) | 30 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 30 | 5 | |
| 83301-0024-2 | Bupropion Hydrochloride (XL) | 90 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 90 | 5 | |
| 83301-0024-3 | Bupropion Hydrochloride (XL) | 500 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 500 | 5 | |
| 83301-0024-4 | Bupropion Hydrochloride (XL) | 1000 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 1000 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 83301-0024 | BUPROPION HYDROCHLORIDE (XL) (BUPROPION HYDROCHLORIDE) TABLET, EXTENDED RELEASE [MULLAN PHAMACEUTICAL INC.] | 2 | Current NDC, 4 package rows | 20241017_75b1e027-4c5d-46e5-98ee-033e67bd411c.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 83301-0024-1 | EA - Each | 83301-0024 | b557931e-0667-4073-b6e1-03bb26e5f257 | 1 | 2025-08-11 |
| 83301-0024-2 | EA - Each | 83301-0024 | 0a488f1f-a008-4823-92e2-8cf1beb41d5b | 1 | 2025-07-08 |
| 83301-0024-3 | EA - Each | 83301-0024 | b4756bd1-7feb-487f-a470-8fcf84089e77 | 1 | 2025-07-08 |
| 83301-0024-4 | EA - Each | 83301-0024 | 0804598b-02f1-414f-a853-b0052a3af713 | 1 | 2025-07-08 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Lights Alcohol Wipes | ISOPROPYL ALCOHOL | Lights Medical Manufacture Co., Ltd. | f9601021-4c52-4b48-96c1-b25fe8fef8b1 | 2026-06-26 | Warnings | ND2M416302 |
| Equate Swimmers Instant Ear Dry | EQUATE SWIMMERS INSTANT EAR DRY | Walmart Stores, Inc | 76b58a7a-48cf-866c-e053-2a91aa0a7e63 | 2026-06-26 | Warnings | ND2M416302 |
| Lights Medium Alcohol | ISOPROPYL ALCOHOL | Lights Medical Manufacture Co., Ltd. | 873e0c9d-e0aa-44bb-a1f4-447458479023 | 2026-06-25 | Warnings | ND2M416302 |
| Bupropion Hydrochloride | BUPROPION HYDROCHLORIDE | St. Mary's Medical Park Pharmacy | 362504fd-2f0a-c097-e063-6394a90ac0fc | 2026-06-25 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Bupropion Hydrochloride | BUPROPION HYDROCHLORIDE | American Health Packaging | 88c980c8-aaa8-4378-9ac2-24d588640caa | 2026-06-24 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| BuPROPion Hydrochloride | BUPROPION HYDROCHLORIDE | American Health Packaging | 1af890f7-1db8-4dd2-bf66-2b1e0c93a3d8 | 2026-06-24 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Swab Applicator Brushes Iodine (0.7% Available Iodine) and Isopropyl Alcohol (74% w/w) | IODINE, ISOPROPYL ALCOHOL | XINXIANG XINDA TECHNOLOGY CO.,LTD | 54e83df5-bbeb-d068-e063-6394a90ad513 | 2026-06-23 | Warnings | ND2M416302 |
| 70% | ISOPROPYL ALCOHOL | ADUSA Distribution, LLC | f340dd7e-6412-4621-a818-2592ca78d0f2 | 2026-06-23 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | ADUSA Distribution, LLC | d95a9736-345b-4b7e-9b24-23edb3cbf7e8 | 2026-06-23 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | ADUSA Distribution, LLC | 7e066163-6629-43ad-b0b8-09c16fe94a0d | 2026-06-23 | Warnings, Adverse reactions | ND2M416302 |
| Bupropion Hydrochloride SR | BUPROPION HYDROCHLORIDE | REMEDYREPACK INC. | c76f2f9f-3999-4bdd-8ec3-e0066318d378 | 2026-06-22 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Isopropyl Rubbing Alcohol 70 | ISOPROPYL ALCOHOL | Delon Laboratories (1990) Ltd. | fb481568-0c51-421f-9b73-adb4c84645aa | 2026-06-22 | Warnings | ND2M416302 |
| Medline | ISOPROPYL ALCOHOL | Medline Industries, LP | 495076e9-3187-6bfa-e063-6394a90a01f5 | 2026-06-22 | Warnings | ND2M416302 |
| Bupropion Hydrochloride SR | BUPROPION HYDROCHLORIDE | Northwind Health Company, LLC | 0865f8cf-1d7f-0e67-e063-6294a90a2f4d | 2026-06-19 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Rohto Sun and Sport | HYPROMELLOSE, POVIDONE | The Mentholatum Company | 8bcc8882-b886-4b55-9bc4-d4b92a41358f | 2026-06-19 | Warnings | FZ989GH94E |
| Rohto Dual Light Relief | HYPROMELLOSE, POVIDONE | The Mentholatum Company | 1b597f83-d7f1-cf93-e063-6394a90a99f7 | 2026-06-19 | Warnings | FZ989GH94E |
| Isopropyl alcohol 91 percent | ISOPROPYL ALCOHOL | P & L Development, LLC | fcda76cb-63c4-4e81-9e0a-13be506a8150 | 2026-06-17 | Warnings | ND2M416302 |
| H-Scars Formula | CALENDULA OFFICINALLIS, SILICEA | Healing Natural Oils LLC | 8433ff00-d815-45e0-b0ec-1448668dd8f8 | 2026-06-16 | Warnings | ETJ7Z6XBU4 |
| E-Z-GAS II | ANTACID/ANTIFLATULENT | E-Z-EM, INC. | 4e12e1cb-b033-076d-e054-00144ff8d46c | 2026-06-15 | Warnings | ETJ7Z6XBU4 |
| BM BIO28 ALCOHOL | CALC SULPH, CALC FLUOR, CALC PHOS, FERR PHOS, KALI MUR, KALI PHOS, KALI SULPH, MAG PHOS, NAT PHOS, NAT SULPH, NAT MUR, SILICEA | Total Operations Management LLC DBA:Bestmade Natural Products Micro | 544b66c4-49df-556f-e063-6394a90af3ed | 2026-06-15 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.