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Promethazine Hydrochloride
Promethazine Hydrochloride - 0703-2201-04 - (Promethazine Hydrochloride)
Drug Information of Promethazine Hydrochloride
| Product NDC: | 0703-2201 |
| Proprietary Name: | Promethazine Hydrochloride |
| Non Proprietary Name: | Promethazine Hydrochloride |
| Active Ingredient(s): | 50 mg/mL & nbsp; Promethazine Hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Promethazine Hydrochloride
| Product NDC: | 0703-2201 |
| Labeler Name: | Teva Parenteral Medicines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040454 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20021001 |
Package Information of Promethazine Hydrochloride
| Package NDC: | 0703-2201-04 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 CARTON (0703-2201-04) > 1 mL in 1 VIAL, SINGLE-DOSE (0703-2201-01) |
NDC Information of Promethazine Hydrochloride
| NDC Code | 0703-2201-04 |
| Proprietary Name | Promethazine Hydrochloride |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (0703-2201-04) > 1 mL in 1 VIAL, SINGLE-DOSE (0703-2201-01) |
| Product NDC | 0703-2201 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Promethazine Hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20021001 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc |
| Substance Name | PROMETHAZINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
