Dextrose Monohydrate is a Parenteral Injection in the Human Prescription Drug category. It is labeled and distributed by International Medication Systems, Limited. The primary component is Dextrose Monohydrate.
| Product ID | 76329-3301_872f0955-2da1-49c0-8b21-8f48115ef533 |
| NDC | 76329-3301 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Dextrose Monohydrate |
| Generic Name | Dextrose Monohydrate |
| Dosage Form | Injection |
| Route of Administration | PARENTERAL |
| Marketing Start Date | 2000-06-01 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | International Medication Systems, Limited |
| Substance Name | DEXTROSE MONOHYDRATE |
| Active Ingredient Strength | 500 mg/mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2000-06-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2000-06-01 |
| Ingredient | Strength |
|---|---|
| DEXTROSE MONOHYDRATE | 500 mg/mL |
| SPL SET ID: | 3a9d9c4a-5e4e-4bb6-b2a9-55e1b0b98f02 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 76329-3301 | Dextrose Monohydrate | Dextrose Monohydrate |
| 71872-7176 | Dextrose Monohydrate | Dextrose Monohydrate |
| 51662-1453 | DEXTROSE MONOHYDRATE | DEXTROSE MONOHYDRATE |
| 51662-1493 | DEXTROSE MONOHYDRATE | DEXTROSE MONOHYDRATE |
| 0338-0017 | DEXTROSE | DEXTROSE MONOHYDRATE |
| 0338-0023 | DEXTROSE | DEXTROSE MONOHYDRATE |
| 0338-0062 | DEXTROSE | dextrose monohydrate |
| 0338-0066 | DEXTROSE | dextrose monohydrate |
| 0338-0070 | DEXTROSE | dextrose monohydrate |
| 0338-0074 | DEXTROSE | dextrose monohydrate |
| 0338-0078 | DEXTROSE | dextrose monohydrate |
| 0338-0082 | DEXTROSE | dextrose monohydrate |