NDC 83301-0025-04 - 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
- 83301-0025
- Requested NDC
- 83301-0025-04
- Package NDCs from labels
- 83301-0025-1, 83301-0025-2, 83301-0025-3, 83301-0025-4, 83301-0025-04
- 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 |
|---|---|---|---|---|---|---|
| 83301-0025-1 | Bupropion Hydrochloride (XL) | 30 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 30 | 5 | |
| 83301-0025-2 | Bupropion Hydrochloride (XL) | 90 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 90 | 5 | |
| 83301-0025-3 | Bupropion Hydrochloride (XL) | 500 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 500 | 5 | |
| 83301-0025-4 | 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 |
|---|---|---|---|---|
| 83301-0025 | 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 |
|---|---|---|---|---|---|
| 83301-0025-1 | EA - Each | 83301-0025 | 8e47748d-71d2-4388-9344-f9f0d0fc85ef | 1 | 2025-08-11 |
| 83301-0025-2 | EA - Each | 83301-0025 | a78b6919-3fad-498c-923b-6eb7466cedc6 | 1 | 2025-07-08 |
| 83301-0025-3 | EA - Each | 83301-0025 | 2ce134ef-bbd6-4df7-b9b6-8f2a7c319497 | 1 | 2025-07-08 |
| 83301-0025-4 | EA - Each | 83301-0025 | 6d41ddf6-32f9-4c91-8680-7630e178d23e | 1 | 2025-08-11 |
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 |
|---|---|---|---|---|---|---|
| Aurum Hypericum | AURUM HYPERICUM | Uriel Pharmacy Inc | be0da1f0-06a1-11df-8a39-0800200c9a66 | 2025-01-10 | Warnings | ETJ7Z6XBU4 |
| Alcohol Prep Pad-Large | ISOPROPYL ALCOHOL | Global Biomedical Technologies, LLC | 93d00515-e93f-48a3-b66b-7d933e734e54 | 2025-01-10 | Warnings | ND2M416302 |
| AM-9 | SPIGELIA ANTHELMIA, SILICON DIOXIDE, AND CORALLIUM RUBRUM WHOLE | DNA Labs, Inc. | d7a00f0b-de4c-4bff-b8e0-86a82bed8bb9 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
| N-8 | SILICON DIOXIDE, ATROPA BELLADONNA, CITRULLUS COLOCYNTHIS FRUIT PULP, BLACK COHOSH, ANEMONE PULSATILLA, SEPIA OFFICINALIS JUICE, PALLADIUM, APIS MELLIFERA, AND BOS TAURUS OVARY | DNA Labs, Inc. | c25cdcb5-9469-48bb-b216-0a9d8d644e12 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
| N-23 | ANEMONE PULSATILLA, PHOSPHORUS, SILICON DIOXIDE, NITRIC ACID, ARSENIC TRIOXIDE, TOXICODENDRON PUBESCENS WHOLE, AND BOS TAURUS HYPOTHALAMUS | DNA Labs, Inc. | b6365b49-06fb-4692-96f7-a5097b70bc91 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
| N-16 | MGO ENERGIZER | DNA Labs, Inc. | 8292b900-86c1-47ea-81da-b587439c7664 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
| N-21 | CALCIUM FLUORIDE, SILICON DIOXIDE, EUPHRASIA STRICTA, RUTA GRAVEOLENS WHOLE, GELSEMIUM SEMPERVIRENS WHOLE, PHYSOSTIGMA VENENOSUM WHOLE, ANEMONE PULSATILLA, SODIUM CHLORIDE, AND SUS SCROFA EYE | DNA Labs, Inc. | 89967941-c4ee-4598-a66d-8a93d69a4d65 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
| N-18 | OYSTER SHELL CALCIUM CARBONATE, CRUDE, SEPIA OFFICINALIS JUICE, SILICON DIOXIDE, NITRIC ACID, AND SUS SCROFA PINEAL GLAND | DNA Labs, Inc. | 3565c5d5-dc68-4f3f-99ec-30f8952393e0 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
| N-24 | METABOLIN | DNA Labs, Inc. | 559fca2b-1093-4bdf-be70-c453f87002c3 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
| NO-WEAK-NAILS | GRAPHITE, THUJA OCCIDENTALIS LEAFY TWIG, AND SILICON DIOXIDE | Miers Laboratories | 9158cd3f-4c27-40e9-bc07-fd560375c3a1 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
| Ferrum Silicicum Urtica | FERRUM SILICICUM URTICA | Uriel Pharmacy Inc. | 09829ac4-c074-7315-e063-6394a90adf59 | 2025-01-07 | Warnings | ETJ7Z6XBU4 |
| bupropion Hydrochloride | BUPROPION HYDROCHLORIDE | Bryant Ranch Prepack | 4971c3cb-07c4-4c65-a16a-f1700e523147 | 2025-01-06 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| bupropion Hydrochloride | BUPROPION HYDROCHLORIDE | Bryant Ranch Prepack | bd99969d-03d5-4609-88e8-a9ae93a83907 | 2025-01-06 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Bupropion Hydrochloride | BUPROPION HYDROCHLORIDE | NuCare Pharmaceuticals,Inc. | 0e8b2109-8516-2d92-e063-6394a90a5d16 | 2025-01-03 | Boxed warning, Warnings, Adverse reactions | 993541 ZG7E5POY8O |
| Signature Care Alcohol Prep Pad | ISOPROPYL ALCOHOL | Better Living Brands LLC | adc87331-1aa1-3457-e053-2a95a90a7eb1 | 2025-01-03 | Warnings | ND2M416302 |
| Alcohol Extra-Thick | ISOPROPYL ALCOHOL | Meijer Distribution Inc | 0b02643d-ea14-4877-ae9c-f0749d1b2d10 | 2025-01-03 | Warnings | ND2M416302 |
| Premier Value | ISOPROPYL ALCOHOL | Pharmacy Value Alliance, LLC | d2baa47e-9673-7f23-e053-2a95a90adcb7 | 2025-01-03 | Warnings | ND2M416302 |
| CVS Alcohol Prep | ISOPROPYL ALCOHOL | CVS Pharmacy | 88f761c1-cb50-4edc-9a54-43444378eff7 | 2025-01-03 | Warnings | ND2M416302 |
| Sterile Alcohol | ISOPROPYL ALCOHOL | Chain Drug Marketing Association Inc | 55922632-3768-4450-9389-ba7d7d91f2c9 | 2025-01-03 | Warnings | ND2M416302 |
| MIMIBO PREMIUM TOOTH | SILICON DIOXIDE, TOCOPHEROL ACETATE, TETRASODIUM PYROPHOSPHATE | CONE MEDICAL Co., Ltd. | c0ff5df4-0b37-0b1b-e053-2a95a90a862c | 2025-01-02 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.