calcium gluceptate
Calcium Gluceptate is a medication used to treat Duodenal Ulcer, Dyspepsia, Peptic Esophagitis, Gastroesophageal Reflux.
Generic · by Lilly
Key facts
- Active ingredient
- Calcium Gluceptate
- Form
- Injectable
- Strength
- Calcium Gluceptate EQ 90MG CALCIUM/5ML
- Type
- Prescription (Rx)
- Brand or generic
- Generic
- May treat
- duodenal ulcer, dyspepsia, peptic esophagitis
- Manufacturer
- Lilly
- FDA application
- NDA006470
- Availability
- Discontinued (per FDA)
May treat (source: NIH RxClass)
Dosage forms
Injectable
The forms currently marketed in the U.S., per the FDA National Drug Code Directory.
Ways to save
Ask for the generic
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Request a 90-day supply
Bulk fills usually lower the per-dose price vs monthly refills.
Use copay cards
Manufacturer copay cards & patient-assistance programs — especially for brand drugs.
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Frequently asked questions
- What does Calcium Gluceptate treat?
- Calcium Gluceptate (Calcium Gluceptate) may be used to treat duodenal ulcer, dyspepsia, peptic esophagitis, gastroesophageal reflux, heart arrest, heartburn, based on NIH RxClass drug-classification data (conditions a drug may treat — not a verbatim copy of the FDA-approved label). This is general reference, not medical advice.
- Is there a coupon or discount for Calcium Gluceptate?
- pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Calcium Gluceptate. To pay less, Calcium Gluceptate is already a generic — usually the lowest-cost version — so the main levers are comparing cash prices between pharmacies and using a pharmacy discount-card service. Prices vary by pharmacy, insurance, and location, so always confirm at the counter. This is general reference, not medical or financial advice.
- Who makes Calcium Gluceptate?
- Calcium Gluceptate is marketed by Lilly. You can see Lilly's full profile, rating, and other products on pharmaranks.
- Is Calcium Gluceptate a brand-name or generic drug?
- Calcium Gluceptate is a generic medication; its active ingredient is Calcium Gluceptate. Generics contain the same active ingredient as the brand-name original and are usually lower cost.
- Is Calcium Gluceptate available over the counter?
- No. Calcium Gluceptate is a prescription (Rx) medication in the US — you need a prescription from a licensed clinician (in person or via telehealth); it isn't sold over the counter. For some conditions there are OTC alternatives — ask your pharmacist.
- What forms does Calcium Gluceptate come in?
- Calcium Gluceptate is currently marketed as injectable, per the FDA's National Drug Code Directory.
- Is Calcium Gluceptate FDA-registered?
- Calcium Gluceptate is on record with the U.S. FDA under application number NDA006470. You can verify this on its official FDA label.
Information is sourced from public FDA regulatory data. Provided for general reference only — not medical advice. Always consult a licensed professional and the current prescribing information.
What people report to the FDA about Calcium Gluceptate
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 50 reports naming Calcium Gluceptate, and the FDA flagged 92% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:
- pyrexia8 reports
- abdominal discomfort7 reports
- amnesia7 reports
- confusional state7 reports
- contusion7 reports
- diarrhoea7 reports
- drug-induced liver injury7 reports
- fatigue7 reports
Read these as a signal, not a rate. A report does not mean Calcium Gluceptate caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label.
Source: openFDA drug/event (FAERS), retrieved September 25, 2026.
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