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Papaverine Hydrochloride
Papaverine Hydrochloride - 0517-4002-25 - (Papaverine Hydrochloride)
Drug Information of Papaverine Hydrochloride
| Product NDC: | 0517-4002 |
| Proprietary Name: | Papaverine Hydrochloride |
| Non Proprietary Name: | Papaverine Hydrochloride |
| Active Ingredient(s): | 30 mg/mL & nbsp; Papaverine Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Papaverine Hydrochloride
| Product NDC: | 0517-4002 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19950901 |
Package Information of Papaverine Hydrochloride
| Package NDC: | 0517-4002-25 |
| Package Description: | 25 VIAL in 1 CARTON (0517-4002-25) > 2 mL in 1 VIAL |
NDC Information of Papaverine Hydrochloride
| NDC Code | 0517-4002-25 |
| Proprietary Name | Papaverine Hydrochloride |
| Package Description | 25 VIAL in 1 CARTON (0517-4002-25) > 2 mL in 1 VIAL |
| Product NDC | 0517-4002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Papaverine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19950901 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | American Regent, Inc. |
| Substance Name | PAPAVERINE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
