NDC 80425-0300-02 - Bupropion hydrochloride
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
- 80425-0300
- Requested NDC
- 80425-0300-02
- Package NDCs from labels
- 80425-0300-1, 80425-0300-2, 80425-0300-3, 80425-0300-02
- Manufacturer
- Advanced Rx Pharmacy of Tennessee, LLC
- Effective date
- 2024-12-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Bupropion hydrochloride - Advanced Rx Pharmacy of Tennessee, LLC | Advanced Rx Pharmacy of Tennessee, LLC | 2024-12-31 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 80425-0300-1 | Bupropion hydrochloride | 30 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 30 | 2 | |
| 80425-0300-2 | Bupropion hydrochloride | 60 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 60 | 2 | |
| 80425-0300-3 | Bupropion hydrochloride | 90 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 90 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 80425-0300 | BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE [ADVANCED RX PHARMACY OF TENNESSEE, LLC] | 2 | Current NDC, 3 package rows | 20250102_f8af7829-8b61-6785-e053-6294a90af052.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 80425-0300-1 | EA - Each | 80425-0300 | 06c687a0-1094-4799-8d6b-b8ef329ae7fc | 1 | 2023-06-06 |
| 80425-0300-2 | EA - Each | 80425-0300 | 65286faa-05d1-4b75-b630-143099f53618 | 1 | 2023-06-06 |
| 80425-0300-3 | EA - Each | 80425-0300 | 4c1c0dea-98d1-4af5-afb5-3243327e47a0 | 1 | 2023-06-06 |
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 | Apotex Corp | 86530199-999b-9f92-b1bc-b8515ec829f3 | 2026-09-09 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| bupropion hydrochloride | BUPROPION HYDROCHLORIDE | REMEDYREPACK INC. | 136f29fa-a859-4efb-8365-1382716d6f8f | 2026-09-03 | Boxed warning, Warnings, Adverse reactions | 993541 ZG7E5POY8O |
| Bupropion Hydrochloride | BUPROPION HYDROCHLORIDE | REMEDYREPACK INC. | 81d251aa-a8e8-493e-94ed-12f6fb8902e6 | 2026-09-02 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Bupropion HCL ER(SR) | BUPROPION HCL ER(SR) | DriectRx | 50afb442-e7c6-d28c-e063-6294a90a2b7e | 2026-08-31 | Warnings, Adverse reactions | ZG7E5POY8O |
| Bupropion hydrochloride | BUPROPION HYDROCHLORIDE | Granules Pharmaceuticals Inc. | d9eb0939-63c1-48c4-a444-a899d7924d06 | 2026-08-27 | Boxed warning, Warnings, Adverse reactions | 993557 993541 ZG7E5POY8O |
| Bupropion hydrochloride | BUPROPION HYDROCHLORIDE | REMEDYREPACK INC. | 0b041720-a25d-403e-a72c-601a8bdd8051 | 2026-08-27 | Boxed warning, Warnings, Adverse reactions | 993557 ZG7E5POY8O |
| Bupropion Hydrochloride SR | BUPROPION HYDROCHLORIDE | REMEDYREPACK INC. | b47c5515-a438-40bc-b8ad-26a6cf9676b7 | 2026-08-27 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Bupropion hydrochloride | BUPROPION HYDROCHLORIDE | REMEDYREPACK INC. | 6087100f-3ba4-412e-b08d-768d1dcdaf00 | 2026-08-27 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Bupropion hydrochloride | BUPROPION HYDROCHLORIDE | REMEDYREPACK INC. | 0aa86bd6-b37b-45f7-a837-b067e41184e9 | 2026-08-27 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Bupropion Hydrochloride XL | BUPROPION HYDROCHLORIDE | REMEDYREPACK INC. | bcbef1b4-a135-4231-bc65-7d0b335260e8 | 2026-08-26 | Boxed warning, Warnings, Adverse reactions | 993557 ZG7E5POY8O |
| Bupropion Hydrochloride XL | BUPROPION HYDROCHLORIDE | Quallent Pharmaceuticals Health LLC | 56df4e22-81ca-48a4-a8e2-038448417355 | 2026-08-25 | Boxed warning, Warnings, Adverse reactions | 993557 993541 ZG7E5POY8O |
| Bupropion Hydrochloride SR | BUPROPION HYDROCHLORIDE | Aphena Pharma Solutions - Tennessee, LLC | 5f8b3313-0286-499f-9235-02cdc0eb063b | 2026-08-25 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Bupropion Hydrochloride | BUPROPION HYDROCHLORIDE | Aphena Pharma Solutions - Tennessee, LLC | 334e5635-e4cc-cf2a-e063-6294a90ae1e1 | 2026-08-24 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Bupropion Hydrochloride (XL) | BUPROPION HYDROCHLORIDE | REMEDYREPACK INC. | 0cd6e0e2-6b2c-4e0d-b5b2-ebfe0d5e31c4 | 2026-08-20 | Boxed warning, Warnings, Adverse reactions | 993541 ZG7E5POY8O |
| AUVELITY | DEXTROMETHORPHAN HYDROBROMIDE, BUPROPION HYDROCHLORIDE | Axsome Therapeutics, Inc. | dcefda7c-9a68-278e-e053-2995a90aec79 | 2026-08-17 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| bupropion hydrochloride SR | BUPROPION HYDROCHLORIDE | Cardinal Health 107, LLC | 439a7e93-f578-434f-943f-4b93c35450f5 | 2026-08-12 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Bupropion Hydrochloride | BUPROPION HYDROCHLORIDE | Coupler LLC | 5829a2aa-4845-b58b-e063-6294a90ad2f4 | 2026-08-03 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Bupropion Hydrochloride (XL) | BUPROPION HYDROCHLORIDE | REMEDYREPACK INC. | 4cc3327b-92c5-4667-ae16-3e95eafcf4d8 | 2026-07-27 | Boxed warning, Warnings, Adverse reactions | 993557 ZG7E5POY8O |
| Bupropion Hydrochloride (XL) | BUPROPION HYDROCHLORIDE | Preferred Pharmaceuticals Inc. | 30c370c2-f2b7-4335-ba55-e8c8f4059092 | 2026-07-24 | Boxed warning, Warnings, Adverse reactions | 993557 ZG7E5POY8O |
| BUPROPION HYDROCHLORIDE | BUPROPION HYDROCHLORIDE | REMEDYREPACK INC. | 080853c0-fcab-4645-9ddc-4946e895ac5f | 2026-07-24 | Boxed warning, Warnings, Adverse reactions | ANDA210497 993541 ZG7E5POY8O |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.