NDC 0406-0357-23 - 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
- 0406-0357
- Requested NDC
- 0406-0357-23
- Package NDCs from labels
- 0406-0357-23
- Manufacturer
- Physicians Total Care, Inc.
- Effective date
- 2014-04-03
- 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. | 2014-04-03 | HUMAN PRESCRIPTION DRUG LABEL |
| HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLETS USP CIII | Liberty Pharmaceuticals, Inc. | 2013-09-09 | HUMAN PRESCRIPTION DRUG LABEL |
| HYDROCODONE BITARTRATE AND ACETAMINOPHEN - Medsource Pharmaceuticals | Medsource Pharmaceuticals | 2012-07-24 | HUMAN PRESCRIPTION DRUG LABEL |
| HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLETS USP CIII | STAT Rx USA LLC | PSS World Medical Inc. | 2012-01-31 | HUMAN PRESCRIPTION DRUG LABEL |
| HYDROCODONE BITARTRATE AND ACETAMINOPHEN - Contract Pharmacy Services-PA | Contract Pharmacy Services-PA | 2012-01-23 | HUMAN PRESCRIPTION DRUG LABEL |
| HYDROCODONE BITARTRATE AND ACETAMINOPHEN - STAT RX USA LLC | STAT RX USA LLC | 2010-06-29 | HUMAN PRESCRIPTION DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2013-03-03 | Indexing - Billing Unit |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0406-0357-01 | EA - Each | 0406-0357 | 5e99876e-18d3-4aab-bb1f-a29985e52f67 | 1 | 2012-07-24 |
| 0406-0357-05 | EA - Each | 0406-0357 | cf68f85b-0a2e-4c78-b3c5-784d4f5d751d | 1 | 2012-07-24 |
| 0406-0357-09 | EA - Each | 0406-0357 | 06374d9c-9f07-4a1a-9388-c722618ccd1b | 1 | 2012-07-24 |
| 0406-0357-23 | EA - Each | 0406-0357 | ed749a1a-614e-44a2-b052-4e92c16e8a8d | 1 | 2013-03-03 |
| 0406-0357-62 | EA - Each | 0406-0357 | a2a0c72b-664a-4de5-a43e-c3235fb5c80e | 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 |
|---|---|---|---|---|---|---|
| Acetaminophen and Codeine Phosphate | ACETAMINOPHEN AND CODEINE PHOSPHATE | Proficient Rx LP | 5d9123f6-b322-4fa0-bf48-6335a6adcbb8 | 2025-01-01 | Warnings, Adverse reactions | 362O9ITL9D |
| Headache, Circle K | ACETAMINOPHEN, CAFFEINE, ASPIRIN TABLET | Lil' Drug Store Products, Inc. | e711ff0a-2fa0-1f2a-e053-2a95a90a4e38 | 2024-12-31 | Warnings | 362O9ITL9D |
| Extra Strength Headache, Lil Drug Store | EXTRA STRENGHT HEADACHE RELIEF- ACETAMINOPHEN, ASPIRIN, CAFFEINE TABLET | Lil' Drug Store Products, Inc. | 0c41deda-490b-f5d2-e063-6394a90a5047 | 2024-12-31 | Warnings | 362O9ITL9D |
| Extra Strength Headache, Circle K | ACETAMINOPHEN/ASPIRIN/CAFFEINE TABLET | Lil' Drug Store Products, Inc. | d18e1631-de43-4b29-e053-2995a90af56d | 2024-12-31 | Warnings | 362O9ITL9D |
| Pain Reliever | ACETAMINOPHEN 500 MG, FILM-COATED TABLET | Lil' Drug Store Products, Inc. | e5f9def4-4cf5-4e06-e053-2995a90a07ea | 2024-12-31 | Warnings | 362O9ITL9D |
| Regular Strength Pain Relief | ACETAMINOPHEN | Geri-Care Pharmaceutical Corp | 6158e954-32d8-4718-e053-2a91aa0a27f3 | 2024-12-31 | Warnings | 362O9ITL9D |
| Acetaminophen | EXTRA STRENGTH PAIN RELIEF | NuCare Pharmaceuticals,Inc. | a32f346e-71d0-cc11-e053-2a95a90ae88c | 2024-12-31 | Warnings | 362O9ITL9D |
| Butalbital/Acetaminophen/Caffeine | BUTALBITAL/ACETAMINOPHEN/CAFFEINE | Advanced Rx Pharmacy of Tennessee, LLC | f16429e2-4944-5bbc-e053-2a95a90ab528 | 2024-12-31 | Warnings, Adverse reactions | 362O9ITL9D |
| Extra Strength Headache Relief | ACETAMINOPHEN, ASPIRIN, AND CAFFEINE | Dollar General | 4907056d-6013-46b1-ae86-469dc3001591 | 2024-12-31 | Warnings | 362O9ITL9D |
| DAYTIME COLD AND FLU MULTI SYMPTOM | DAYTIME COLD AND FLU MULTI SYMPTOM | TARGET CORP | 9dea350d-2f09-b944-e053-2995a90a2b63 | 2024-12-30 | Warnings | 362O9ITL9D |
| Pediacare Childrens Grape | ACETAMINOPHEN | RANDOB LABS,LTD. DBA CROSSINGWELL CONSUMER HEALTH | f9d531a2-234c-4feb-8f05-212dbee83dfe | 2024-12-30 | Warnings | 362O9ITL9D |
| Pediacare Childrens Acetaminophen Grape | ACETAMINOPHEN | RANDOB LABS,LTD. DBA CROSSINGWELL CONSUMER HEALTH | 596372c7-eca3-4527-8e22-ab0751e2526b | 2024-12-30 | Warnings | 362O9ITL9D |
| Cold and Flu Nighttime Severe | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | Lil' Drug Store Products, Inc. | ef6836fa-d104-d7b3-e053-2a95a90af2b8 | 2024-12-30 | Warnings | 362O9ITL9D |
| Extra Strength Pain Reliever | ACETAMINOPHEN 500 MG, FILM-COATED CAPLET | Lil' Drug Store Products, Inc. | e5fd2b46-683e-4cf5-e053-2995a90a5512 | 2024-12-30 | Warnings | 362O9ITL9D |
| Night Time Severe Cold and Cough Relief | ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL | Chain Drug Consortium, LLC | c8e9b57b-83e9-46c5-9791-02c4c2b94004 | 2024-12-29 | Warnings | 362O9ITL9D |
| Acetaminophen | ACETAMINOPHEN | CVS Pharmacy | 6f880abe-5284-42b0-9db6-b071444b197b | 2024-12-27 | Warnings | 362O9ITL9D |
| Acetaminophen | ACETAMINOPHEN | CHAIN DRUG MARKETING ASSOCIATION INC. | 1608b4f0-bf20-4024-b8f2-20a4df7a4b21 | 2024-12-26 | Warnings | 362O9ITL9D |
| Aacetaminophen and Ibuprofen | ACETAMINOPHEN AND IBUPROFEN | GRANULES USA, INC. | 1dd90684-6505-8e07-e063-6394a90afdf4 | 2024-12-26 | Warnings | 362O9ITL9D |
| ACETAMINOPHEN | ACETAMINOPHEN | CHAIN DRUG MARKETING ASSOCIATION INC | cfc7eac3-35be-4002-b8ef-be1dfc8caf69 | 2024-12-26 | Warnings | 362O9ITL9D |
| ACETAMINOPHEN | ACETAMINOPHEN | CHAIN DRUG MARKETING ASSOCIATION INC | a3031139-4709-43f2-95a8-89840c595f7f | 2024-12-26 | Warnings | 362O9ITL9D |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.