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meperidine hydrochloride
meperidine hydrochloride - 57664-467-08 - (meperidine hydrochloride)
Drug Information of meperidine hydrochloride
| Product NDC: | 57664-467 |
| Proprietary Name: | meperidine hydrochloride |
| 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 meperidine hydrochloride
| Product NDC: | 57664-467 |
| Labeler Name: | Caraco Pharmaceutical Laboratories, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040446 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070104 |
Package Information of meperidine hydrochloride
| Package NDC: | 57664-467-08 |
| Package Description: | 100 TABLET in 1 BOTTLE (57664-467-08) |
NDC Information of meperidine hydrochloride
| NDC Code | 57664-467-08 |
| Proprietary Name | meperidine hydrochloride |
| Package Description | 100 TABLET in 1 BOTTLE (57664-467-08) |
| Product NDC | 57664-467 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | meperidine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070104 |
| Marketing Category Name | ANDA |
| Labeler Name | Caraco Pharmaceutical Laboratories, Ltd. |
| Substance Name | MEPERIDINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
