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 |
|---|---|---|---|---|---|---|
| Bupropion hydrochloride | BUPROPION HYDROCHLORIDE | BluePoint Laboratories | 4956af38-182a-4015-a945-67e40bd38772 | 2026-01-28 | Boxed warning, Warnings, Adverse reactions | 993557 993541 ZG7E5POY8O |
| Singular Wipes Unscented | ISOPROPYL ALCOHOL | SINGULAR ENTERPRISES LLC | ac2b352f-6cb2-4683-bb41-13e8ecb186bf | 2026-01-27 | Warnings | ND2M416302 |
| Snap Labs Ammonia Inhalants | AMMONIA INHALANT | Brined LLC d/b/a Snap Labs | 4927c18f-078e-94ec-e063-6394a90a4c6d | 2026-01-24 | Warnings | 5138Q19F1X |
| Everlit Survival Sting Relief Pad | ISOPROPYL ALCOHOL | EVERLIT GLOBAL INC. | 3a0414ea-f862-aa0f-e063-6294a90aecb7 | 2026-01-23 | Warnings | ND2M416302 |
| EVERLIT SURVIVAL PREP PAD | ISOPROPYL ALCOHOL | EVERLIT GLOBAL INC. | 3a03ed81-5b1d-172e-e063-6394a90ac59c | 2026-01-23 | Warnings | ND2M416302 |
| Rite Aid Isopropyl Alcohol Wipes | ISOPROPYL ALCOHOL | Rite Aid | bca837b0-5044-4e97-e053-2a95a90a13af | 2026-01-22 | Warnings | ND2M416302 |
| BioMicroneedle PDRN Cream | SILICON DIOXIDE | Guangzhou Shengyanghui Industrial Trading Co., Ltd | 48e2edae-94ea-c42e-e063-6394a90a907b | 2026-01-21 | Warnings | ETJ7Z6XBU4 |
| Lights Isopropyl Alcohol Prep Pads | ISOPROPYL ALCOHOL | Lights Medical Manufacture Co., Ltd. | 4905a27c-6cf8-4b1a-a02c-4c81756e8c0a | 2026-01-21 | Warnings | ND2M416302 |
| LIGHTS Instant Sting Relief Pad | BENZOCAINE | Lights Medical Manufacture Co., Ltd. | 28dd82a7-f360-a022-e063-6394a90a3a76 | 2026-01-21 | Warnings | ND2M416302 |
| DOP Isopropyl Rubbing Alcohol 70% | ISOPROPYL ALCOHOL | Omega & Delta Co., Inc. | c779a35b-1118-4560-8d77-6878edb4c267 | 2026-01-21 | Warnings | ND2M416302 |
| Inflammation I | ECHINACEA (ANGUSTIFOLIA), NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, HYDRASTIS CANADENSIS, APIS MELLIFICA, BELLADONNA, FERRUM PHOSPHORICUM, NITRICUM ACIDUM, OLEANDER, SILICEA | BioActive Nutritional, Inc. | 3cb12181-ae7e-45c7-a1b1-e1952f36f8c3 | 2026-01-21 | Warnings | ETJ7Z6XBU4 |
| Bupropion hydrochloride | BUPROPION HYDROCHLORIDE | Preferred Pharmaceuticals Inc. | 093c4a61-02d9-4b55-b612-569aa25d3f2a | 2026-01-20 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Bupropion Hydrochloride SR | BUPROPION HYDROCHLORIDE | ScieGen Pharmaceuticals, Inc. | 092da413-ec60-4577-ac57-51e3e42d55c9 | 2026-01-19 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Bupropion Hydrochloride SR | BUPROPION HYDROCHLORIDE | Northwind Health Company, LLC | f2b3939b-a410-6354-e053-2995a90ababb | 2026-01-19 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Bupropion Hydrochloride SR | BUPROPION HYDROCHLORIDE | Radha Pharmaceuticals, Inc. | 161637d2-bc9d-4a2b-ad1f-6cc39ffd69ce | 2026-01-19 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | ATOSAFE CO., Ltd | 487c5036-0eb0-ada9-e063-6394a90aa02e | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | DONG IL PHARMS CO.,LTD | 487cd5b9-28f3-392d-e063-6394a90a9ba1 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO GUM CARE COOL MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | ATOSAFE CO., Ltd | 487cf27a-d761-6353-e063-6394a90af029 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | ATOSAFE CO., Ltd | 487d52d1-8853-bc90-e063-6394a90ab91d | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO GUM CARE COOL MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | DONG IL PHARMS CO.,LTD | 487d689d-ebdd-43c3-e063-6294a90af0e2 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.