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Papaverine Hydrochloride
Papaverine Hydrochloride - 66758-014-02 - (Papaverine Hydrochloride)
Drug Information of Papaverine Hydrochloride
| Product NDC: | 66758-014 |
| Proprietary Name: | Papaverine Hydrochloride |
| Non Proprietary Name: | Papaverine Hydrochloride |
| Active Ingredient(s): | 30 mg/mL & nbsp; Papaverine Hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Papaverine Hydrochloride
| Product NDC: | 66758-014 |
| Labeler Name: | Ebewe Parenta Pharmaceuticals Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 20081201 |
Package Information of Papaverine Hydrochloride
| Package NDC: | 66758-014-02 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (66758-014-02) > 2 mL in 1 VIAL, SINGLE-DOSE (66758-014-01) |
NDC Information of Papaverine Hydrochloride
| NDC Code | 66758-014-02 |
| Proprietary Name | Papaverine Hydrochloride |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (66758-014-02) > 2 mL in 1 VIAL, SINGLE-DOSE (66758-014-01) |
| Product NDC | 66758-014 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Papaverine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20081201 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | Ebewe Parenta Pharmaceuticals Inc |
| Substance Name | PAPAVERINE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
