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Hydrocodone Bitatrate and Acetaminophen
Hydrocodone Bitatrate and Acetaminophen - 65084-453-10 - (Hydrocodone Bitatrate and Acetaminophen)
Drug Information of Hydrocodone Bitatrate and Acetaminophen
| Product NDC: | 65084-453 |
| Proprietary Name: | Hydrocodone Bitatrate and Acetaminophen |
| Non Proprietary Name: | Hydrocodone Bitatrate and Acetaminophen |
| Active Ingredient(s): | 325; 10 mg/1; mg/1 & nbsp; Hydrocodone Bitatrate and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocodone Bitatrate and Acetaminophen
| Product NDC: | 65084-453 |
| Labeler Name: | Rx Pak Division of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040148 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130624 |
Package Information of Hydrocodone Bitatrate and Acetaminophen
| Package NDC: | 65084-453-10 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (65084-453-10) |
NDC Information of Hydrocodone Bitatrate and Acetaminophen
| NDC Code | 65084-453-10 |
| Proprietary Name | Hydrocodone Bitatrate and Acetaminophen |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (65084-453-10) |
| Product NDC | 65084-453 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitatrate and Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130624 |
| Marketing Category Name | ANDA |
| Labeler Name | Rx Pak Division of McKesson Corporation |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 325; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
