Home
>
National Drug Code (NDC)
>
Maxidone
Maxidone - 52544-634-05 - (Hydrocodone Bitartrate and Acetaminophen)
Drug Information of Maxidone
| Product NDC: | 52544-634 |
| Proprietary Name: | Maxidone |
| Non Proprietary Name: | Hydrocodone Bitartrate and Acetaminophen |
| Active Ingredient(s): | 750; 10 mg/1; mg/1 & nbsp; Hydrocodone Bitartrate and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Maxidone
| Product NDC: | 52544-634 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040094 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990322 |
Package Information of Maxidone
| Package NDC: | 52544-634-05 |
| Package Description: | 500 TABLET in 1 BOTTLE (52544-634-05) |
NDC Information of Maxidone
| NDC Code | 52544-634-05 |
| Proprietary Name | Maxidone |
| Package Description | 500 TABLET in 1 BOTTLE (52544-634-05) |
| Product NDC | 52544-634 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitartrate and Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19990322 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 750; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
