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 |