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DEXTROSE

NDC 51662-1215 · HF Acquisition Co LLC, DBA HealthFirst

Generic nameDEXTROSE
Dosage formINJECTION, SOLUTION
RouteINTRAVENOUS
Active ingredient(s)DEXTROSE MONOHYDRATE
Strength25 g/50mL
Marketing categoryNDA

Packages

51662-1215-1 — 50 mL in 1 VIAL, SINGLE-DOSE (51662-1215-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43203-852 — Anticoagulant Citrate Dextrose A ACD-A, 46163-206 — dextrose monohydrate, sodium chloride, sodium lactate, calcium chloride, magnesium chloride, 46163-209 — dextrose monohydrate, sodium chloride, sodium lactate, calcium chloride, magnesium chloride, 46163-212 — dextrose monohydrate, sodium chloride, sodium lactate, calcium chloride, magnesium chloride, 49230-188 — Dextrose Monohydrate, Sodium Chloride, Sodium Lactate, Calcium Chloride, Magnesium Chloride, 49230-191 — Dextrose Monohydrate, Sodium Chloride, Sodium Lactate, Calcium Chloride, Magnesium Chloride, 49230-206 — Dextrose Monohydrate, Sodium Chloride, Sodium Lactate, Calcium Chloride, Magnesium Chloride, 49230-209 — Dextrose Monohydrate, Sodium Chloride, Sodium Lactate, Calcium Chloride, Magnesium Chloride, 49230-212 — Dextrose Monohydrate, Sodium Chloride, Sodium Lactate, Calcium Chloride, Magnesium Chloride, 51662-1213 — 25% Dextrose Infant, 51662-1216 — 50% DEXTROSE, 51662-1453 — DEXTROSE MONOHYDRATE, 51662-1521 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, AND DEXTROSE MONOHYDRATE, 51662-1584 — Dextrose monohydrate, 51662-1680 — DEXTROSE, 53877-108 — Anhydrous Citric Acid, Trisodium Citrate Dihydrate, Sodium Phosphate, Monobasic, Monohydrate, Dextrose Monohydrate, and Adenine, 53877-109 — Anhydrous Citric Acid, Trisodium Citrate Dihydrate, Sodium Phosphate, Monobasic, Monohydrate, Dextrose Monohydrate, and Adenine, 53877-110 — Anhydrous Citric Acid, Trisodium Citrate Dihydrate, Sodium Phosphate, Monobasic, Monohydrate, Dextrose Monohydrate, and Adenine, 63323-624 — Dextrose Monohydrate, 63323-667 — Potassium Chloride, Dextrose Monohydrate, +185 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels