NDC 60505-0158-01 - 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
- 60505-0158
- Requested NDC
- 60505-0158-01
- Package NDCs from labels
- 60505-0158-3, 60505-0158-9, 60505-0158-1, 60505-0158-5, 60505-0158-7, 60505-0158-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-09-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Bupropion Hydrochloride - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-09-24 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - PD-Rx Pharmaceuticals, Inc. | PD-Rx Pharmaceuticals, Inc. | 2026-09-23 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - Apotex Corp | Apotex Inc. | Apotex Corp | Apotex Inc. | 2026-09-09 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - Major Pharmaceuticals | Major Pharmaceuticals | 2026-03-03 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - AvPAK | AvPAK | 2026-02-24 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - Golden State Medical Supply, Inc. | Golden State Medical Supply, Inc. | 2025-11-18 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - Bryant Ranch Prepack | Bryant Ranch Prepack | 2025-08-26 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - Bryant Ranch Prepack | Bryant Ranch Prepack | 2025-07-14 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2024-07-17 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - Proficient Rx LP | Proficient Rx LP | 2024-07-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - Medsource Pharmaceuticals | Apotex Inc. | Medsource Pharmaceuticals | Apotex Inc. | 2024-03-13 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2020-01-21 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - Aphena Pharma Solutions - Tennessee, LLC | Aphena Pharma Solutions - Tennessee, LLC | 2020-01-21 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - Unit Dose Services | Unit Dose Services | 2019-09-21 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - Contract Pharmacy Services-PA | Coupler Enterprises | Contract Pharmacy Services-PA | Coupler Enterprises | 2017-09-18 | HUMAN PRESCRIPTION DRUG LABEL |
| Bupropion Hydrochloride - NCS HealthCare of KY, Inc dba Vangard Labs | NCS HealthCare of KY, Inc dba Vangard Labs | 2015-01-06 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 60505-0158-1 | Bupropion Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 22 | |
| 60505-0158-3 | Bupropion Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 22 | |
| 60505-0158-5 | Bupropion Hydrochloride | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | 22 | |
| 60505-0158-7 | Bupropion Hydrochloride | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | 22 | |
| 60505-0158-9 | Bupropion Hydrochloride | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 22 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 60505-0158 | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [APOTEX CORP] | 18 | Current NDC, Legacy NDC, 5 package rows | 20240523_86530199-999b-9f92-b1bc-b8515ec829f3.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 60505-0158-1 | EA - Each | 60505-0158 | c53dc1e1-33a2-469d-9acc-938b4a9ec11a | 1 | 2012-07-24 |
| 60505-0158-5 | EA - Each | 60505-0158 | 6c4fc750-14e9-411a-91bc-cded606d076b | 1 | 2012-07-24 |
| 60505-0158-9 | EA - Each | 60505-0158 | a041eab0-6dd1-4b99-b207-7f1b977168e6 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| Q Skin Science | SUNSCREEN | International Cosmeceuticals, Inc | 59e4c3d0-ee4c-2350-e063-6394a90ac9d2 | 2026-08-25 | Warnings | 15FIX9V2JP |
| MELAO zinc stick(GREEN) | TITANIUM DIOXIDE,ZINC OXIDE,OCTOCRYLENE | Guangzhou Haishi Biological Technology Co., Ltd. | 59c70c82-f7ff-9a04-e063-6294a90a7b3d | 2026-08-24 | Warnings | 15FIX9V2JP |
| Bupropion Hydrochloride | BUPROPION HYDROCHLORIDE | Aphena Pharma Solutions - Tennessee, LLC | 334e5635-e4cc-cf2a-e063-6294a90ae1e1 | 2026-08-24 | Boxed warning, Warnings, Adverse reactions | 993691 ZG7E5POY8O |
| SKIN-INFUSED FOUNDATION SPF 25/ Mineral sunscreen broad Spectrum SPF 25 01 | ZINC OXIDE, TITANIUM DIOXIDE | Cosmuses Cosmetics (Ningbo) Co., Ltd. | 59d74e3f-e3fa-a7a9-e063-6294a90a76e5 | 2026-08-24 | Warnings | 15FIX9V2JP |
| Aging Eye Formula | CINERARIA MARITIMA, EYE (SUIS), CALCAREA FLUORICA, CAUSTICUM, PHOSPHORUS, SILICEA, ZINCUM METALLICUM, GERMANIUM METALLICUM, NATRUM MURIATICUM | Nutritional Specialties, Inc. | d5b44f79-5299-4b31-ba45-0e511cdbe17c | 2026-08-24 | Warnings | ETJ7Z6XBU4 |
| Rohto All-In-One | HYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE | The Mentholatum Company | 43e690e4-b381-46e3-838c-33aef5bdadde | 2026-08-20 | Warnings | 3NXW29V3WO |
| Bio Combination 28 | SCHUESSLER SALTS | LDD Bioscience Private Limited | 597caf33-5107-9dec-e063-6294a90a5fcd | 2026-08-20 | Warnings | ETJ7Z6XBU4 |
| Sweat Resistant Sunscreen Body Original | TITANIUM DIOXIDE, ZINC OXIDE | Clutch, Inc. | 4bbde755-e312-123e-e063-6294a90a467f | 2026-08-20 | Warnings | 15FIX9V2JP |
| Bupropion Hydrochloride (XL) | BUPROPION HYDROCHLORIDE | REMEDYREPACK INC. | 0cd6e0e2-6b2c-4e0d-b5b2-ebfe0d5e31c4 | 2026-08-20 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| Psorinum Complex | PHOSPHORUS, SILICEA, SULPHUR, ALOE | BioActive Nutritional, Inc. | d4746927-e6d4-463d-a084-56ffc48d1e67 | 2026-08-20 | Warnings | ETJ7Z6XBU4 |
| Boneforce HP | CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, HEKLA LAVA, HYDROFLUORICUM ACIDUM, RHUS TOX, SILICEA, SYMPHYTUM OFFICINALE | BioActive Nutritional, Inc. | d96ca52b-781d-431c-ad2a-a54fd57eb106 | 2026-08-20 | Warnings | ETJ7Z6XBU4 |
| HEADHUNTER SURF SCREEN SPF 50 SUNSCREEN | ZINC OXIDE,TITANIUM DIOXIDE | Guangzhou Tata Biotechnology Co., Ltd. | 4339df13-77d3-31a1-e063-6394a90a5208 | 2026-08-17 | Warnings | 15FIX9V2JP |
| Cerebellum Thalamus A Aurm | CEREBELLUM THALAMUS A AURUM | Uriel Pharmacy Inc. | e1c395b8-9221-401f-8980-c91ff8843458 | 2026-08-17 | Warnings | ETJ7Z6XBU4 |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | HAMBLIN DERMATOLOGY | 5942e64c-416e-7525-e063-6394a90a2839 | 2026-08-17 | Warnings | 15FIX9V2JP |
| Protect Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | Opal Day Spa | 5943413a-48e1-0bdf-e063-6294a90a2fff | 2026-08-17 | Warnings | 15FIX9V2JP |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | MedSpa By Beauty Bar LLC | 5943ba3d-688e-9e9c-e063-6294a90afa9a | 2026-08-17 | Warnings | 15FIX9V2JP |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | CORBY, JR., TERRY L. | 594443fd-8e27-4ec6-e063-6294a90a3ff0 | 2026-08-17 | Warnings | 15FIX9V2JP |
| Leader Dry Eye Relief Eye Drops | GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400 | CARDINAL HEALTH 110, LLC. DBA LEADER | 2ded4bda-b3c3-4521-8701-5c8446fd148b | 2026-08-17 | Warnings | 3NXW29V3WO |
| AUVELITY | DEXTROMETHORPHAN HYDROBROMIDE, BUPROPION HYDROCHLORIDE | Axsome Therapeutics, Inc. | dcefda7c-9a68-278e-e053-2995a90aec79 | 2026-08-17 | Boxed warning, Warnings, Adverse reactions | ZG7E5POY8O |
| BM BM134 DROPS | ARSENIC ALBUM, HYDRASTIS, MYRISTICA, NITRIC ACID, PAEONIA, RHUS TOX, SILICEA | BM Private Limited | 59023500-89be-cc76-e063-6294a90a6e02 | 2026-08-14 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.