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Ultra Strength

NDC 30142-108 · KROGER COMPANY

Generic nameCalcium Carbonate
Dosage formTABLET, CHEWABLE
RouteORAL
Active ingredient(s)CALCIUM CARBONATE
Strength1000 mg/1
Pharmacologic classBlood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
Marketing categoryOTC MONOGRAPH DRUG

Packages

30142-108-72 — 72 TABLET, CHEWABLE in 1 BOTTLE (30142-108-72)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

21130-614 — famotidine, calcium carbonate and magnesium hydroxide, 21130-786 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 24385-106 — Calcium Carbonate, 24385-478 — Calcium carbonate, 24385-485 — Calcium Carbonate, 24385-595 — Calcium carbonate, 27854-120 — calcium carbonate, 29485-6522 — famotidine, calcium carbonate, and magnesium hydroxide tablet, chewable, 29485-8120 — calcium carbonate tablet, chewable, 30142-040 — famotidine, calcium carbonate and magnesium hydroxide, 30142-115 — Calcium Carbonate, 30142-162 — Calcium Carbonate, 30142-200 — Calcium Carbonate, 30142-204 — Calcium Carbonate, 30142-207 — Calcium Carbonate, 30142-213 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 30142-267 — Calcium Carbonate, 30142-268 — Calcium Carbonate, 30142-300 — Calcium Carbonate, 30142-307 — Calcium Carbonate, +648 more

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