Home
>
National Drug Code (NDC)
>
Methocarbamol
Methocarbamol - 63739-166-10 - (methocarbamol)
Drug Information of Methocarbamol
| Product NDC: | 63739-166 |
| Proprietary Name: | Methocarbamol |
| Non Proprietary Name: | methocarbamol |
| Active Ingredient(s): | 500 mg/1 & nbsp; methocarbamol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methocarbamol
| Product NDC: | 63739-166 |
| Labeler Name: | McKesson Packaging Services a business unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040489 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070703 |
Package Information of Methocarbamol
| Package NDC: | 63739-166-10 |
| Package Description: | 10 BLISTER PACK in 1 BOX (63739-166-10) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Methocarbamol
| NDC Code | 63739-166-10 |
| Proprietary Name | Methocarbamol |
| Package Description | 10 BLISTER PACK in 1 BOX (63739-166-10) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 63739-166 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methocarbamol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070703 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Packaging Services a business unit of McKesson Corporation |
| Substance Name | METHOCARBAMOL |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
