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Hydrocodone Bitartrate and Acetaminophen
Hydrocodone Bitartrate and Acetaminophen - 17856-1295-1 - (Hydrocodone Bitartrate and Acetaminophen)
Drug Information of Hydrocodone Bitartrate and Acetaminophen
| Product NDC: | 17856-1295 |
| Proprietary Name: | Hydrocodone Bitartrate and Acetaminophen |
| Non Proprietary Name: | Hydrocodone Bitartrate and Acetaminophen |
| Active Ingredient(s): | 500; 7.5 mg/15mL; mg/15mL & nbsp; Hydrocodone Bitartrate and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocodone Bitartrate and Acetaminophen
| Product NDC: | 17856-1295 |
| Labeler Name: | Atlantic Biologicals Corps |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040520 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20031030 |
Package Information of Hydrocodone Bitartrate and Acetaminophen
| Package NDC: | 17856-1295-1 |
| Package Description: | 15 mL in 1 CUP (17856-1295-1) |
NDC Information of Hydrocodone Bitartrate and Acetaminophen
| NDC Code | 17856-1295-1 |
| Proprietary Name | Hydrocodone Bitartrate and Acetaminophen |
| Package Description | 15 mL in 1 CUP (17856-1295-1) |
| Product NDC | 17856-1295 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitartrate and Acetaminophen |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20031030 |
| Marketing Category Name | ANDA |
| Labeler Name | Atlantic Biologicals Corps |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 500; 7.5 |
| Strength Unit | mg/15mL; mg/15mL |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
