Home
>
National Drug Code (NDC)
>
PROMETHAZINE HYDROCHLORIDE
PROMETHAZINE HYDROCHLORIDE - 10019-097-01 - (promethazine hydrochloride)
Drug Information of PROMETHAZINE HYDROCHLORIDE
| Product NDC: | 10019-097 |
| Proprietary Name: | PROMETHAZINE HYDROCHLORIDE |
| Non Proprietary Name: | promethazine hydrochloride |
| Active Ingredient(s): | 25 mg/mL & nbsp; promethazine hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PROMETHAZINE HYDROCHLORIDE
| Product NDC: | 10019-097 |
| Labeler Name: | BAXTER HEALTHCARE CORPORATION |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083312 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091210 |
Package Information of PROMETHAZINE HYDROCHLORIDE
| Package NDC: | 10019-097-01 |
| Package Description: | 25 VIAL in 1 PACKAGE (10019-097-01) > 1 mL in 1 VIAL (10019-097-44) |
NDC Information of PROMETHAZINE HYDROCHLORIDE
| NDC Code | 10019-097-01 |
| Proprietary Name | PROMETHAZINE HYDROCHLORIDE |
| Package Description | 25 VIAL in 1 PACKAGE (10019-097-01) > 1 mL in 1 VIAL (10019-097-44) |
| Product NDC | 10019-097 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | promethazine hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20091210 |
| Marketing Category Name | ANDA |
| Labeler Name | BAXTER HEALTHCARE CORPORATION |
| Substance Name | PROMETHAZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
