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Meperidine Hydrochloride
Meperidine Hydrochloride - 0641-6052-25 - (Meperidine Hydrochloride)
Drug Information of Meperidine Hydrochloride
| Product NDC: | 0641-6052 |
| Proprietary Name: | Meperidine Hydrochloride |
| Non Proprietary Name: | Meperidine Hydrochloride |
| Active Ingredient(s): | 25 mg/mL & nbsp; Meperidine Hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Meperidine Hydrochloride
| Product NDC: | 0641-6052 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080445 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19750122 |
Package Information of Meperidine Hydrochloride
| Package NDC: | 0641-6052-25 |
| Package Description: | 25 VIAL in 1 CARTON (0641-6052-25) > 1 mL in 1 VIAL (0641-6052-01) |
NDC Information of Meperidine Hydrochloride
| NDC Code | 0641-6052-25 |
| Proprietary Name | Meperidine Hydrochloride |
| Package Description | 25 VIAL in 1 CARTON (0641-6052-25) > 1 mL in 1 VIAL (0641-6052-01) |
| Product NDC | 0641-6052 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Meperidine Hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 19750122 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp. |
| Substance Name | MEPERIDINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
