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Meperidine Hydrochloride
Meperidine Hydrochloride - 0555-0382-02 - (Meperidine Hydrochloride)
Drug Information of Meperidine Hydrochloride
| Product NDC: | 0555-0382 |
| Proprietary Name: | Meperidine Hydrochloride |
| Non Proprietary Name: | Meperidine Hydrochloride |
| Active Ingredient(s): | 100 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: | 0555-0382 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088640 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19961011 |
Package Information of Meperidine Hydrochloride
| Package NDC: | 0555-0382-02 |
| Package Description: | 100 TABLET in 1 BOTTLE (0555-0382-02) |
NDC Information of Meperidine Hydrochloride
| NDC Code | 0555-0382-02 |
| Proprietary Name | Meperidine Hydrochloride |
| Package Description | 100 TABLET in 1 BOTTLE (0555-0382-02) |
| Product NDC | 0555-0382 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Meperidine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19961011 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | MEPERIDINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
