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ZYDONE
ZYDONE - 63481-668-70 - (Hydrocodone Bitartrate and Acetaminophen)
Drug Information of ZYDONE
| Product NDC: | 63481-668 |
| Proprietary Name: | ZYDONE |
| Non Proprietary Name: | Hydrocodone Bitartrate and Acetaminophen |
| Active Ingredient(s): | 400; 5 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 ZYDONE
| Product NDC: | 63481-668 |
| Labeler Name: | Endo Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040288 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19981201 |
Package Information of ZYDONE
| Package NDC: | 63481-668-70 |
| Package Description: | 100 TABLET in 1 BOTTLE (63481-668-70) |
NDC Information of ZYDONE
| NDC Code | 63481-668-70 |
| Proprietary Name | ZYDONE |
| Package Description | 100 TABLET in 1 BOTTLE (63481-668-70) |
| Product NDC | 63481-668 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitartrate and Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19981201 |
| Marketing Category Name | ANDA |
| Labeler Name | Endo Pharmaceuticals Inc. |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 400; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
