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Demerol
Demerol - 0024-0335-04 - (Meperidine Hydrochloride)
Drug Information of Demerol
| Product NDC: | 0024-0335 |
| Proprietary Name: | Demerol |
| Non Proprietary Name: | Meperidine Hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; Meperidine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Demerol
| Product NDC: | 0024-0335 |
| Labeler Name: | sanofi-aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA005010 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19421110 |
Package Information of Demerol
| Package NDC: | 0024-0335-04 |
| Package Description: | 100 TABLET in 1 BOTTLE (0024-0335-04) |
NDC Information of Demerol
| NDC Code | 0024-0335-04 |
| Proprietary Name | Demerol |
| Package Description | 100 TABLET in 1 BOTTLE (0024-0335-04) |
| Product NDC | 0024-0335 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Meperidine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19421110 |
| Marketing Category Name | NDA |
| Labeler Name | sanofi-aventis U.S. LLC |
| Substance Name | MEPERIDINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
