Hydrocodone Acetaminophen is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Redpharm Drug Inc.. The primary component is Hydrocodone Bitartrate; Acetaminophen.
| Product ID | 67296-0016_63fa3273-38d3-4855-aa4d-a4ff5b572fd2 |
| NDC | 67296-0016 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Hydrocodone Acetaminophen |
| Generic Name | Hydrocodone, Acetaminophen |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2011-03-03 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA081083 |
| Labeler Name | RedPharm Drug Inc. |
| Substance Name | HYDROCODONE BITARTRATE; ACETAMINOPHEN |
| Active Ingredient Strength | 8 mg/1; mg/1 |
| Pharm Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
| DEA Schedule | CIII |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2011-03-03 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA081083 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-03-03 |
| Inactivation Date | 2019-10-29 |
| Ingredient | Strength |
|---|---|
| HYDROCODONE BITARTRATE | 7.5 mg/1 |
| SPL SET ID: | b165dffd-1550-4d8d-a8ea-fe83512c34e6 |
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