Prescription drug · ANDA
Dextrose (Dextrose monohydrate) NDC 17271-721
Dextrose monohydrate 100 mg/mL · Injection, Solution · Intravenous · Becton Dickinson and Company
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 17271-721-05 | 1727107210517271072105 | 30 BAG in 1 CASE (17271-721-05) / 250 mL in 1 BAGMarketed from Feb 5, 2020 | |
| 17271-721-06 | 1727107210617271072106 | 20 BAG in 1 CASE (17271-721-06) / 500 mL in 1 BAGMarketed from Feb 5, 2020 | |
| 17271-721-07 | 1727107210717271072107 | 10 BAG in 1 CASE (17271-721-07) / 1000 mL in 1 BAGMarketed from Feb 5, 2020 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Dextrose
- Generic name (nonproprietary)
- dextrose monohydrate
- Active ingredients
- Dextrose monohydrate — 100 mg/mL
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Labeler
- Becton Dickinson and CompanyNDC labeler code 17271
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 209448
- Marketing start
- Listing expires
- Identifiers
- Product ID 17271-721_16de339e-70a9-4375-8e4b-31b6313b6666SPL ID 16de339e-70a9-4375-8e4b-31b6313b6666SPL set ID 8e7046f8-841e-465a-af69-af9fb3d6799dRxCUI 1795477, 1795480, 1795481UNII LX22YL083G
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.
- Administration
Drug administration (CPT 96360–96549)
When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.
- NDC on a medical claim
N417271072105followed by a unit qualifier and the quantityPackage 17271-0721-05. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Dextrose Injection is indicated as source of water and calories. Dextrose Injection is indicated as a source of water and calories. ( 1 )
Excerpt only. Read the full label for complete information.
About NDC 17271-721
- What is NDC 17271-721?
- 17271-721 is the product NDC for Dextrose (dextrose monohydrate), Dextrose monohydrate 100 mg/mL injection, solution, listed with the FDA by Becton Dickinson and Company. It has 3 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Dextrose (Dextrose Monohydrate).
- What is the active ingredient?
- Dextrose monohydrate.
- Who is the labeler?
- Becton Dickinson and Company, NDC labeler code 17271. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Dextrose?
- 69 other product NDCs are listed under this name. See all Dextrose NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Dextrose products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Dextrosedextrose monohydrate | Dextrose monohydrate 250 mg/mL | Injection, SolutionIntravenous | REMEDYREPACK INC. | 70518-4452 | 70518-4452-00 |
| Dextrosedextrose monohydrate | Dextrose monohydrate 25 g/50mL | Injection, SolutionIntravenous | REMEDYREPACK INC. | 70518-4219 | 70518-4219-00 |
| Dextrosedextrose monohydrate | Dextrose monohydrate 50 mg/mL | Injection, SolutionIntravenous | FRESENIUS KABI USA, LLC | 65219-456 | 65219-0456-60 |
| Dextrosedextrose monohydrate | Dextrose monohydrate 50 mg/mL | Injection, SolutionIntravenous | FRESENIUS KABI USA, LLC | 65219-458 | 65219-0458-30 |
| Dextrosedextrose monohydrate | Dextrose monohydrate 50 mg/mL | Injection, SolutionIntravenous | FRESENIUS KABI USA, LLC | 65219-460 | 65219-0460-20 |
| Dextrosedextrose monohydrate | Dextrose monohydrate 50 mg/mL | Injection, SolutionIntravenous | FRESENIUS KABI USA, LLC | 65219-462 | 65219-0462-10 |
| Dextrosedextrose monohydrate | Dextrose monohydrate 50 mg/mL | Injection, SolutionIntravenous | FRESENIUS KABI USA, LLC | 65219-464 | 65219-0464-50 |
| Dextrosedextrose monohydrate | Dextrose monohydrate 50 mg/mL | Injection, SolutionIntravenous | ProPharma Distribution | 84549-460 | 84549-0460-20 |
| Dextrosedextrose monohydrate | Dextrose monohydrate 25 g/50mL | Injection, SolutionIntravenous | Henry Schein, Inc. | 0404-9845 | 00404-9845-50 |
| Dextrosedextrose monohydrate | Dextrose monohydrate 25 g/50mL | Injection, SolutionIntravenous | Henry Schein, Inc. | 0404-9847 | 00404-9847-50 |
Other NDCs under ANDA 209448
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Dextrose | Dextrose monohydrate 100 mg/mL | Injection, SolutionIntravenous | HF Acquisition Co. LLC. DBA HealthFirst | 51662-1680 |
| Dextrosedextrose monohydrate | Dextrose monohydrate 100 mg/mL | Injection, SolutionIntravenous | Fresenius Kabi USA, LLC | 63323-824 |