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Duramorph
Duramorph - 0641-6019-10 - (morphine sulfate)
Drug Information of Duramorph
| Product NDC: | 0641-6019 |
| Proprietary Name: | Duramorph |
| Non Proprietary Name: | morphine sulfate |
| Active Ingredient(s): | 1 mg/mL & nbsp; morphine sulfate |
| Administration Route(s): | EPIDURAL; INTRATHECAL; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Duramorph
| Product NDC: | 0641-6019 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018565 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19840918 |
Package Information of Duramorph
| Package NDC: | 0641-6019-10 |
| Package Description: | 10 AMPULE in 1 CARTON (0641-6019-10) > 10 mL in 1 AMPULE (0641-6019-01) |
NDC Information of Duramorph
| NDC Code | 0641-6019-10 |
| Proprietary Name | Duramorph |
| Package Description | 10 AMPULE in 1 CARTON (0641-6019-10) > 10 mL in 1 AMPULE (0641-6019-01) |
| Product NDC | 0641-6019 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | morphine sulfate |
| Dosage Form Name | INJECTION |
| Route Name | EPIDURAL; INTRATHECAL; INTRAVENOUS |
| Start Marketing Date | 19840918 |
| Marketing Category Name | NDA |
| Labeler Name | West-ward Pharmaceutical Corp. |
| Substance Name | MORPHINE SULFATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
