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Bacteriostatic Water
Bacteriostatic Water - 49349-739-01 - (WATER)
Drug Information of Bacteriostatic Water
| Product NDC: | 49349-739 |
| Proprietary Name: | Bacteriostatic Water |
| Non Proprietary Name: | WATER |
| Active Ingredient(s): | 1 mL/mL & nbsp; WATER |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bacteriostatic Water
| Product NDC: | 49349-739 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018802 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130610 |
Package Information of Bacteriostatic Water
| Package NDC: | 49349-739-01 |
| Package Description: | 30 mL in 1 VIAL (49349-739-01) |
NDC Information of Bacteriostatic Water
| NDC Code | 49349-739-01 |
| Proprietary Name | Bacteriostatic Water |
| Package Description | 30 mL in 1 VIAL (49349-739-01) |
| Product NDC | 49349-739 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | WATER |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20130610 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | WATER |
| Strength Number | 1 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
