NDC 54868-3585-2 - HYDROCODONE BITARTRATE AND ACETAMINOPHEN
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
- 54868-3585
- Requested NDC
- 54868-3585-2
- Package NDCs from labels
- 54868-3585-5, 54868-3585-2
- Manufacturer
- Physicians Total Care, Inc.
- Effective date
- 2014-02-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLETS USP CIII | Physicians Total Care, Inc. | 2014-02-17 | HUMAN PRESCRIPTION DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54868-3585-5 | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | 120 in 1 BOTTLE, PLASTIC | TABLET | 120 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 54868-3585 | HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [PHYSICIANS TOTAL CARE, INC.] | 5 | 1 package rows | 20140217_ab52a549-8ecc-441a-8733-0fda146e9932.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 54868-3585-0 | EA - Each | 54868-3585 | c3f7bb28-3883-49b4-9ab7-8a1084cadc9f | 1 | 2012-07-24 |
| 54868-3585-1 | EA - Each | 54868-3585 | 02f5ecde-20a9-45d9-9daf-0458cb4fc6a1 | 1 | 2012-07-24 |
| 54868-3585-2 | EA - Each | 54868-3585 | 9801ac21-07dc-4ae9-a3c4-ea74673ffb1d | 1 | 2012-07-24 |
| 54868-3585-3 | EA - Each | 54868-3585 | 402e281e-0440-40a7-af62-c4ea8810f805 | 1 | 2012-07-24 |
| 54868-3585-5 | EA - Each | 54868-3585 | 73a2c3fa-a4d6-4949-af38-cbf3656dbbc4 | 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 |
|---|---|---|---|---|---|---|
| M-PAP | ACETAMINOPHEN | Method Pharmaceuticals, LLC | 3d1bb61c-15db-4eba-aba9-cfbcbc7b30e0 | 2025-10-21 | Warnings | 362O9ITL9D |
| Hydrocodone Bitartrate and Acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | Bryant Ranch Prepack | ee4b164d-7ee2-4c19-b1a3-cb60c6676786 | 2025-10-21 | Boxed warning, Warnings, Adverse reactions | NO70W886KK 362O9ITL9D |
| Daytime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | United Natural Foods, Inc. dba UNFI | 311e2b6b-21cb-4b4c-a78d-a0732d29602f | 2025-10-21 | Warnings | 362O9ITL9D |
| Hydrocodone Bitartrate and Acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | Bryant Ranch Prepack | 94ba2279-440e-4eaf-ad19-04d90a5c4c10 | 2025-10-21 | Boxed warning, Warnings, Adverse reactions | 857005 NO70W886KK 362O9ITL9D |
| Hydrocodone Bitartrate and Acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | Bryant Ranch Prepack | 177c4cd8-80dd-4ed7-9e12-dcec70e0278e | 2025-10-21 | Boxed warning, Warnings, Adverse reactions | 857005 NO70W886KK 362O9ITL9D |
| iVIZIA Dry Eye | POVIDONE | Thea Pharma Inc. | 1ef73cb1-da48-a713-e063-6294a90afa9d | 2025-10-20 | Warnings | FZ989GH94E |
| Norel AD | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, AND PHENYLEPHRINE HCL | U.S. PHARMACEUTICAL CORPORATION | 53d9ed3c-212d-4b12-ac35-8bd49382b49d | 2025-10-17 | Warnings | 362O9ITL9D |
| Menstrual Complete Maximum Strength | ACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATE | CHAIN DRUG MARKETING ASSOCIATION INC | 913d8bdb-7644-464c-b9a6-55387ff12059 | 2025-10-17 | Warnings | 362O9ITL9D |
| Butalbital And Acetaminophen | BUTALBITAL AND ACETAMINOPHEN | Larken Laboratories, Inc. | 326c83fc-afed-45ad-9c87-f47968fa1d2a | 2025-10-15 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Daytime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Care One (Retail Business Services, LLC.) | 6ca7372b-50c4-4b15-b133-fefa35525ade | 2025-10-15 | Warnings | 362O9ITL9D |
| DENTI BUONGIORNO PEACH MINT WHITENING TOOTH | HYDROGEN PEROXIDE, SILICA | ATOSAFE CO., Ltd | 41196c2f-8e2e-a54d-e063-6294a90ad8a7 | 2025-10-14 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PEACH MINT WHITENING TOOTH | HYDROGEN PEROXIDE, SILICA | DONG IL PHARMS CO.,LTD | 41198822-7c8f-ceb2-e063-6394a90a4373 | 2025-10-14 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO ORIGINAL TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | DONG IL PHARMS CO.,LTD | 41197bb6-f6f4-c86d-e063-6294a90ad476 | 2025-10-14 | Warnings | ETJ7Z6XBU4 |
| ACETAMINOPHEN 500 MG | ACETAMINOPHEN | ASCLEMED USA INC. | db8e6702-88ac-4db2-9dd8-7d0ed997c2b5 | 2025-10-14 | Warnings | 362O9ITL9D |
| Pain Reliever Extra Strength | ACETAMINOPHEN | Walgreen Company | fa33f6ef-522b-4630-9716-92371d9cd24a | 2025-10-14 | Warnings | 362O9ITL9D |
| DENTI BUONGIORNO ORIGINAL TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | ATOSAFE CO., Ltd | 4114ab09-1115-6b0b-e063-6394a90ab442 | 2025-10-13 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PLAQUE CARE TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | ATOSAFE CO., Ltd | 41155922-d7ac-0a7a-e063-6294a90afe48 | 2025-10-13 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PLAQUE CARE TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | DONG IL PHARMS CO.,LTD | 41157552-2473-176b-e063-6294a90a9ad0 | 2025-10-13 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO GUM CARE TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | ATOSAFE CO., Ltd | 4115d122-3090-d3e5-e063-6294a90aafb6 | 2025-10-13 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO GUM CARE TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | DONG IL PHARMS CO.,LTD | 4115b653-63ff-703f-e063-6294a90a652a | 2025-10-13 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.