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Sodium Chloride
Sodium Chloride - 0641-1512-36 - (Sodium Chloride)
Drug Information of Sodium Chloride
| Product NDC: | 0641-1512 |
| Proprietary Name: | Sodium Chloride |
| Non Proprietary Name: | Sodium Chloride |
| Active Ingredient(s): | 9 mg/mL & nbsp; Sodium Chloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Chloride
| Product NDC: | 0641-1512 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201850 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120120 |
Package Information of Sodium Chloride
| Package NDC: | 0641-1512-36 |
| Package Description: | 100 AMPULE in 1 CARTON (0641-1512-36) > 10 mL in 1 AMPULE (0641-1512-10) |
NDC Information of Sodium Chloride
| NDC Code | 0641-1512-36 |
| Proprietary Name | Sodium Chloride |
| Package Description | 100 AMPULE in 1 CARTON (0641-1512-36) > 10 mL in 1 AMPULE (0641-1512-10) |
| Product NDC | 0641-1512 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Chloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20120120 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp. |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | 9 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
