DILUENT is a Intravenous; Subcutaneous Injection in the Human Prescription Drug category. It is labeled and distributed by Sandoz Inc. The primary component is Water.
| Product ID | 0781-6021_19f50f18-7400-4b9f-b97a-49b16c48b207 |
| NDC | 0781-6021 |
| Product Type | Human Prescription Drug |
| Proprietary Name | DILUENT |
| Generic Name | Water Solution |
| Dosage Form | Injection |
| Route of Administration | INTRAVENOUS; SUBCUTANEOUS |
| Marketing Start Date | 2019-03-25 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA203649 |
| Labeler Name | Sandoz Inc |
| Substance Name | WATER |
| Active Ingredient Strength | 1 mL/mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2019-03-25 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA203649 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2019-03-25 |
| Ingredient | Strength |
|---|---|
| WATER | 1 mL/mL |
| SPL SET ID: | 473297ca-a872-4052-a053-87dc8f0d3c13 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0173-0518 | Diluent | water |
| 0173-0857 | Diluent | water |
| 0781-6021 | DILUENT | water solution |
| 49281-912 | Diluent | Sodium Chloride |
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| 73408-936 | Crane Safety Eye Wash | water solution |
| 30142-010 | Eye Wash | water solution |
| 0002-0800 | Sterile Diluent | diluent |