NDC 67296-2201-01 - 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
- 67296-2201
- Requested NDC
- 67296-2201-01
- Package NDCs from labels
- 67296-2201-1, 67296-2201-2, 67296-2201-3, 67296-2201-4, 67296-2201-5, 67296-2201-6, 67296-2201-7, 67296-2201-8, 67296-2201-01
- Manufacturer
- Redpharm Drug
- Effective date
- 2026-03-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hydrocodone Bitartrate and Acetaminophen - Redpharm Drug | Redpharm Drug | 2026-03-03 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 67296-2201-1 | Hydrocodone Bitartrate and Acetaminophen | 4 in 1 BOTTLE | TABLET | 4 | 2 | |
| 67296-2201-2 | Hydrocodone Bitartrate and Acetaminophen | 6 in 1 BOTTLE | TABLET | 6 | 2 | |
| 67296-2201-3 | Hydrocodone Bitartrate and Acetaminophen | 10 in 1 BOTTLE | TABLET | 10 | 2 | |
| 67296-2201-4 | Hydrocodone Bitartrate and Acetaminophen | 15 in 1 BOTTLE | TABLET | 15 | 2 | |
| 67296-2201-5 | Hydrocodone Bitartrate and Acetaminophen | 20 in 1 BOTTLE | TABLET | 20 | 2 | |
| 67296-2201-6 | Hydrocodone Bitartrate and Acetaminophen | 30 in 1 BOTTLE | TABLET | 30 | 2 | |
| 67296-2201-7 | Hydrocodone Bitartrate and Acetaminophen | 40 in 1 BOTTLE | TABLET | 40 | 2 | |
| 67296-2201-8 | Hydrocodone Bitartrate and Acetaminophen | 12 in 1 BOTTLE | TABLET | 12 | 2 |
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 |
|---|---|---|---|---|---|---|
| HEADACHE HP | SILVER NITRATE, ATROPA BELLADONNA, BRYONIA ALBA ROOT, GELSEMIUM SEMPERVIRENS ROOT, NITROGLYCERIN, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, MELILOTUS OFFICINALIS TOP, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, SILICON DIOXIDE, SPIGELIA ANTHELMIA | Natural Creations, Inc. | c38b83f0-3918-4ef6-8dfd-48fe438e584a | 2025-12-12 | Warnings | ETJ7Z6XBU4 |
| Acetaminophen | ACETAMINOPHEN | PAI Holdings, LLC dba PAI Pharma | 33599f18-5f49-4f22-8a77-a072115763ef | 2025-12-11 | Warnings | 362O9ITL9D |
| Sinus Congestion and Pain Relief Non-Drowsy | ACETAMINOPHEN, PHENYLEPHRINE HCL | WinCo Foods, LLC | f7e925f4-7da6-4157-a97f-e6a3e399911f | 2025-12-11 | Warnings | 362O9ITL9D |
| Menstrual Complete | ACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATE | WinCo Foods, LLC | 860c4e94-1d1a-4f74-a14a-35f86f4523c4 | 2025-12-11 | Warnings | 362O9ITL9D |
| Hydrocodone Bitartrate and Acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | Redpharm Drug | 37451478-b961-873b-e063-6394a90a7b4e | 2025-12-11 | Boxed warning, Warnings, Adverse reactions | NO70W886KK 362O9ITL9D |
| Cell Well | CALCIUM CARBONICA,CALCIUM FLUORATUM,CALCIUM PHOSPHORICUM,CALCIUM SULPHURICUM,FERRUM PHOSPHORICUM,KALIUM MURIATICUM,KALIUM PHOSPHORICUM,KALIUM SULPHURICUM,MAGNESIUM CARBONICA,MAGNESIUM PHOSPHORICUM,NATRUM MURIATICUM,NATRUM PHOSPHORICUM,NATRUM SULPHURICUM,SILICEA | JoyWell Co LLC | 592c1f48-21c8-4ff5-8818-046662c9effe | 2025-12-11 | Warnings | ETJ7Z6XBU4 |
| Sinus Relief Severe Congestion and Pain | ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | CARDINAL HEALTH | 645f8075-e33f-4e1a-9249-7368261cdcb9 | 2025-12-11 | Warnings | 362O9ITL9D |
| Extra Strength Pain Relief PM | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | VALU MERCHANDISERS COMPANY | f8820150-feec-4062-85bb-14525ddf691f | 2025-12-11 | Warnings | 362O9ITL9D |
| Extra Strength Pain Relief | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | 005e299e-aa84-49d9-bbca-12236f865a27 | 2025-12-11 | Warnings | 362O9ITL9D |
| Mucus Relief Sinus Severe Congestion Relief | ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | VALU MERCHANDISERS COMPANY | 2e751d67-51b4-4b74-a9e8-7f3bc5636984 | 2025-12-11 | Warnings | 362O9ITL9D |
| Pressure and Pain Plus Mucus PE | ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | VALU MERCHANDISERS COMPANY | 232acb86-7383-4992-b333-1e47bf7c06ad | 2025-12-11 | Warnings | 362O9ITL9D |
| Extra Strength Pain Relief | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | d4c32e70-778a-4d66-b9d0-03944a528421 | 2025-12-11 | Warnings | 362O9ITL9D |
| Sinus Pressure plus Pain PE | ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE | VALU MERCHANDISERS COMPANY | 72847721-9f59-4af1-8f20-dc8449742918 | 2025-12-11 | Warnings | 362O9ITL9D |
| Cold plus Flu Severe | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | VALU MERCHANDISERS COMPANY | f6401317-0295-14b3-e053-2a95a90acbb4 | 2025-12-11 | Warnings | 362O9ITL9D |
| Head Congestion plus Flu Severe PE | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | VALU MERCHANDISERS COMPANY | f6401b58-8cf8-4067-e053-2995a90a68fc | 2025-12-11 | Warnings | 362O9ITL9D |
| 8 Hour Arthritis Pain | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | cd3a7094-ddb5-4583-a1bc-dc6ce280418c | 2025-12-11 | Warnings | 362O9ITL9D |
| Extra Strength Pain Relief | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | 5a80cb17-7731-4457-acd3-64cf4accf862 | 2025-12-11 | Warnings | 362O9ITL9D |
| 8 Hour Pain Relief | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | d11a7412-a543-0e34-e053-2995a90afd63 | 2025-12-11 | Warnings | 362O9ITL9D |
| Sinus Relief Pressure, Pain and Cough | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | VALU MERCHANDISERS COMPANY | b1ba37b8-4558-0808-e053-2995a90a9f5e | 2025-12-11 | Warnings | 362O9ITL9D |
| Acetaminophen | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | 02e3798f-86d9-64b4-e063-6294a90a29de | 2025-12-11 | Warnings | 362O9ITL9D |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.