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Phenergan
Phenergan - 60977-002-04 - (PROMETHAZINE HYDROCHLORIDE)
Drug Information of Phenergan
| Product NDC: | 60977-002 |
| Proprietary Name: | Phenergan |
| Non Proprietary Name: | PROMETHAZINE HYDROCHLORIDE |
| Active Ingredient(s): | 50 mg/mL & nbsp; PROMETHAZINE HYDROCHLORIDE |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenergan
| Product NDC: | 60977-002 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083312 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091210 |
Package Information of Phenergan
| Package NDC: | 60977-002-04 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 PACKAGE (60977-002-04) > 1 mL in 1 VIAL, SINGLE-DOSE (60977-002-44) |
NDC Information of Phenergan
| NDC Code | 60977-002-04 |
| Proprietary Name | Phenergan |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 PACKAGE (60977-002-04) > 1 mL in 1 VIAL, SINGLE-DOSE (60977-002-44) |
| Product NDC | 60977-002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PROMETHAZINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20091210 |
| Marketing Category Name | ANDA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | PROMETHAZINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
