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Hydromorphone Hydrochloride
Hydromorphone Hydrochloride - 0641-0121-25 - (Hydromorphone Hydrochloride)
Drug Information of Hydromorphone Hydrochloride
| Product NDC: | 0641-0121 |
| Proprietary Name: | Hydromorphone Hydrochloride |
| Non Proprietary Name: | Hydromorphone Hydrochloride |
| Active Ingredient(s): | 2 mg/mL & nbsp; Hydromorphone Hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydromorphone Hydrochloride
| Product NDC: | 0641-0121 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19720101 |
Package Information of Hydromorphone Hydrochloride
| Package NDC: | 0641-0121-25 |
| Package Description: | 25 VIAL in 1 CARTON (0641-0121-25) > 1 mL in 1 VIAL (0641-0121-21) |
NDC Information of Hydromorphone Hydrochloride
| NDC Code | 0641-0121-25 |
| Proprietary Name | Hydromorphone Hydrochloride |
| Package Description | 25 VIAL in 1 CARTON (0641-0121-25) > 1 mL in 1 VIAL (0641-0121-21) |
| Product NDC | 0641-0121 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydromorphone Hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 19720101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | West-ward Pharmaceutical Corp. |
| Substance Name | HYDROMORPHONE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
