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Promethazine Hydrochloride
Promethazine Hydrochloride - 0409-2312-31 - (PROMETHAZINE HYDROCHLORIDE)
Drug Information of Promethazine Hydrochloride
| Product NDC: | 0409-2312 |
| 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: | 0409-2312 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040372 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091001 |
Package Information of Promethazine Hydrochloride
| Package NDC: | 0409-2312-31 |
| Package Description: | 10 CARTRIDGE in 1 BOX (0409-2312-31) > 1 mL in 1 CARTRIDGE |
NDC Information of Promethazine Hydrochloride
| NDC Code | 0409-2312-31 |
| Proprietary Name | Promethazine Hydrochloride |
| Package Description | 10 CARTRIDGE in 1 BOX (0409-2312-31) > 1 mL in 1 CARTRIDGE |
| Product NDC | 0409-2312 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PROMETHAZINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20091001 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | PROMETHAZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
