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DEMEROL
DEMEROL - 0409-1201-20 - (MEPERIDINE HYDROCHLORIDE)
Drug Information of DEMEROL
| Product NDC: | 0409-1201 |
| Proprietary Name: | DEMEROL |
| Non Proprietary Name: | MEPERIDINE HYDROCHLORIDE |
| Active Ingredient(s): | 100 mg/mL & nbsp; MEPERIDINE HYDROCHLORIDE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DEMEROL
| Product NDC: | 0409-1201 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021171 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101130 |
Package Information of DEMEROL
| Package NDC: | 0409-1201-20 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 BOX (0409-1201-20) > 20 mL in 1 VIAL, MULTI-DOSE |
NDC Information of DEMEROL
| NDC Code | 0409-1201-20 |
| Proprietary Name | DEMEROL |
| Package Description | 1 VIAL, MULTI-DOSE in 1 BOX (0409-1201-20) > 20 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 0409-1201 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MEPERIDINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20101130 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | MEPERIDINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
