Gemcitabine 100 MG/ML Injectable Solution — RxCUI 1998783
RxNorm drug concept · Semantic clinical drug
RxCUI 1998783
Semantic clinical drug · SCD
● Current RxNorm concept 3 FDA products
3 package NDCs
Snapshot Jul 14, 2026
What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.
🗂️ Key Facts
RxCUI1998783
Official nameGemcitabine 100 MG/ML Injectable Solution
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
FDA products mapped3
Package NDCs mapped3
Reported Medicaid activity (SDUD)223 prescriptions · 8 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Gemcitabine Injection: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- Gemcitabine is used to treat four types of cancer: advanced ovarian cancer that has come back after platinum-based chemo, metastatic breast cancer (combined with paclitaxel), non-s...
- You'll receive gemcitabine through an IV (into a vein) at a clinic or infusion center — it's not a pill you take at home. Each infusion takes about 30 minutes, and it's typically g...
- How is gemcitabine given, and what should I expect during infusion?
- The most common side effects include nausea, vomiting, fatigue from low red blood cells, fever, rash, and swelling. Your blood counts will often drop during treatment, which is exp...
🕸️ Concept Web — How Gemcitabine 100 MG/ML Injectable Solution Connects
One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept
Gemcitabine 100 MG/ML Injectable Solution
RxCUI 1998783 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
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Ingredients 1
The active substance itself — no strength, form, or brand attached yet.
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Gemcitabine
12574IN
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Gemcitabine
-
Dose forms 4
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Gemcitabine Injectable Solution
1998782SCDF -
Gemcitabine Injectable Product
1156710SCDG -
Injectable Solution
316949DF -
Injectable Product
1151126DFG
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Gemcitabine Injectable Solution
-
Clinical & branded drugs 1
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Gemcitabine 100 MG/ML
1998781SCDC
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Gemcitabine 100 MG/ML
Showing up to 8 concepts per family — 6 of 6 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.
🔀 Generic ⇄ Brand Crosswalk
The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.
Generic (Clinical) Concepts
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Gemcitabine 100 MG/ML
SCDC · 1998781 -
Gemcitabine Injectable Solution
SCDF · 1998782 -
Gemcitabine Injectable Product
SCDG · 1156710
📦 FDA Products & Package NDCs
3 products · 3 package NDCs
3 package NDCs map to RxCUI 1998783 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
| Package NDC | Package | Brand / generic name | Labeler | Marketing start |
|---|---|---|---|---|
| 68001-0342-34 | 1 VIAL, MULTI-DOSE in 1 CARTON (68001-342-34) / 2 mL in 1 V... | GEMCITABINE | BluePoint Laboratories | 2018-05-25 |
| 68001-0348-36 | 1 VIAL, MULTI-DOSE in 1 CARTON (68001-348-36) / 10 mL in 1... | GEMCITABINE | BluePoint Laboratories | 2018-05-25 |
| 68001-0359-37 | 1 VIAL, MULTI-DOSE in 1 CARTON (68001-359-37) / 20 mL in 1... | GEMCITABINE | BluePoint Laboratories | 2018-05-25 |
Observed labelers:
BluePoint Laboratories (3)
— this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.
🗃️ Sources & Limits
Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
- A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
- Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
- Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
- Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.