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Rabeloc IV Injection

NAFDAC Reg. No. A4-0721 · Drug

Registered with NAFDAC. Registration activeAs of 27 October 2026 · synced automatically from official sources.
Product
Rabeloc IV Injection
NAFDAC number
A4-0721
Active ingredient
Rabeprazole Sodium
Strength
20 mg
Form
Powder for injection
Pack size
1 x 1's (in vial)
Manufacturer
Not listed
Applicant (holder)
Interpharma Industries Limited
Approved
28 Oct 2021
Status
Active View on NAFDAC ↗
Registration valid to
27 Oct 2026
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Rabeloc IV Injection is on the NAFDAC register with an active registration (A4-0721). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

What Rabeloc IV Injection is used for

From the official U.S. FDA label for rabeprazole sodium, the active ingredient registered with NAFDAC.

What it is used for

Rabeprazole sodium delayed-release tablets are a proton pump inhibitor (PPI) indicated in adults for: Healing of Erosive or Ulcerative Gastroesophageal Reflux Disease (GERD). ( 1.1 ) Maintenance of Healing of Erosive or Ulcerative GERD. ( 1.2 ) Treatment of Symptomatic GERD. ( 1.3 ) Healing of Duodenal Ulcers. ( 1.4 ) Helicobacter pylori Eradication to Reduce Risk of Duodenal Ulcer Recurrence. ( 1.5 ) Treatment of Pathological Hypersecretory Conditions, Including Zollinger-Ellison Syndrome. ( 1.6 ) In adolescent patients 12 years of age and older for: Short-term Treatment of Symptomatic GERD. …

Possible side effects

The following serious adverse reactions are described below and elsewhere in labeling: Acute Tubulointerstitial Nephritis [see Warnings and Precautions (5.3) ]. Clostridium difficile -Associated Diarrhea [see Warnings and Precautions (5.4) ]. Bone Fracture [see Warnings and Precautions (5.5) ]. Cutaneous and Systemic Lupus Erythematosus [see Warnings and Precautions (5.7) ]. Cyanocobalamin (Vitamin B-12) Deficiency [see Warnings and Precautions (5.8) ]. Hypomagnesemia and Mineral Metabolism [see Warnings and Precautions (5.9) ]. Fundic Gland Polyps [see Warnings and Precautions (5.11) ]. …

Do not use if

Rabeprazole delayed-release sodium tablets are contraindicated in patients with known hypersensitivity to rabeprazole, substituted benzimidazoles, or to any component of the formulation. Hypersensitivity reactions may include anaphylaxis, anaphylactic shock, angioedema, bronchospasm, acute tubulointerstitial nephritis, and urticaria [see Warnings and Precautions (5.3) , Adverse Reactions (6) ]. …

Warnings

Gastric Malignancy: In adults, symptomatic response to therapy with rabeprazole does not preclude the presence of gastric malignancy. Consider additional follow-up and diagnostic testing. ( 5.1 ) Use with Warfarin: Monitor for increases in INR and prothrombin time. ( 5.2 , 7 ) Acute Tubulointerstitial Nephritis: Discontinue treatment and evaluate patients. ( 5.3 ) Clostridium difficile- Associated Diarrhea: PPI therapy may be associated with increased risk of Clostridium difficile- Associated Diarrhea. ( 5.4 ) Bone Fracture: Long-term and multiple daily dose PPI therapy may be associated with an increased risk for osteoporosis-related fractures of the hip, wrist, or spine. …

Pregnancy & breastfeeding

IN SPECIFIC POPULATIONS Pediatric Use : Dosage strength not appropriate for patients less than 12 years. ( 2 , 8.4 ) 8.1 Pregnancy Risk Summary There are no available human data on rabeprazole sodium use in pregnant women to inform the drug associated risk. The background risk of major birth defects and miscarriage for the indicated populations are unknown. However, the background risk in the U.S. …

General information only, not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

Check your pack of Rabeloc IV Injection

Add the expiry date on your pack for a full Trust Score.

3 free checks left today Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Rabeloc IV Injection

What is in Rabeloc IV Injection?

Rabeloc IV Injection contains Rabeprazole Sodium (20 mg), as powder for injection, according to its NAFDAC registration record.

Is Rabeloc IV Injection registered with NAFDAC?

Yes. Rabeloc IV Injection is listed on the NAFDAC register under registration number A4-0721, and its registration is active as of 27 October 2026.

Has Rabeloc IV Injection been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Rabeloc IV Injection in our automatically synced alert list.

How can I check that my pack of Rabeloc IV Injection is genuine?

Run a free authenticity scan with the NAFDAC number A4-0721, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

What is Rabeloc IV Injection used for?

Rabeprazole sodium delayed-release tablets are a proton pump inhibitor (PPI) indicated in adults for: Healing of Erosive or Ulcerative Gastroesophageal Reflux Disease (GERD). ( 1.1 ) Maintenance of Healing of Erosive or Ulcerative GERD. ( 1.2 ) Treatment of Symptomatic GERD. ( 1.3 ) Healing of Duodenal Ulcers. ( 1.4 ) Helicobacter pylori Eradication to Reduce Risk of Duodenal Ulcer Recurrence. ( 1 (Summarised from the official U.S. FDA label for rabeprazole sodium. Always follow your doctor or pharmacist.)

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