United States · FDA National Drug Code directory
Calcium Acetate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 62135-192_2471197e-c8a7-c3c7-e063-6394a90a16d7
- Product NDC
- 62135-192
- Form
- TABLET
- Composition / generic term
- Calcium Acetate
- Labeler
- Chartwell RX LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190701
- Source listing expiry
- 20261231
Source-listed ingredients
- CALCIUM ACETATE — 667 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 200 TABLET in 1 BOTTLE (62135-192-22) · 62135-192-22
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →