marc glassman ultra strength

Generic: calcium carbonate

Labeler: marc glassman, inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name marc glassman ultra strength
Generic Name calcium carbonate
Labeler marc glassman, inc
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

calcium carbonate 1000 mg/1

Manufacturer
MARC GLASSMAN, INC

Identifiers & Regulatory

Product NDC 68998-103
Product ID 68998-103_3f263ceb-18cb-5b09-e063-6394a90a1890
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2019-04-17

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68998103
Hyphenated Format 68998-103

Supplemental Identifiers

RxCUI
308892
UNII
H0G9379FGK

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name marc glassman ultra strength (source: ndc)
Generic Name calcium carbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (68998-103-72)
source: ndc

Packages (1)

Ingredients (1)

calcium carbonate (1000 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f263ceb-18cb-5b09-e063-6394a90a1890", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["35372a73-9578-4f46-9005-019fd8dd2e18"], "manufacturer_name": ["MARC GLASSMAN, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (68998-103-72)", "package_ndc": "68998-103-72", "marketing_start_date": "20190417"}], "brand_name": "Marc Glassman Ultra Strength", "product_id": "68998-103_3f263ceb-18cb-5b09-e063-6394a90a1890", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "68998-103", "generic_name": "Calcium Carbonate", "labeler_name": "MARC GLASSMAN, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Marc Glassman", "brand_name_suffix": "Ultra Strength", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190417", "listing_expiration_date": "20261231"}