berkley jensen ultra strength

Generic: antacid calcium carbonate

Labeler: bjwc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name berkley jensen ultra strength
Generic Name antacid calcium carbonate
Labeler bjwc
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

calcium carbonate 1000 mg/1

Manufacturer
BJWC

Identifiers & Regulatory

Product NDC 68391-033
Product ID 68391-033_c7eedcbf-3b07-4cd3-937b-c56d7cc5bc57
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2025-03-17

Pharmacologic Class

Classes
blood coagulation factor [epc] calcium [cs] cations divalent [cs] increased coagulation factor activity [pe] phosphate binder [epc] phosphate chelating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68391033
Hyphenated Format 68391-033

Supplemental Identifiers

RxCUI
308892
UPC
0000000000000
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 berkley jensen ultra strength (source: ndc)
Generic Name antacid calcium carbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 265 TABLET, CHEWABLE in 1 BOTTLE (68391-033-65)
source: ndc

Packages (1)

68391-033-65 265 TABLET, CHEWABLE in 1 BOTTLE (68391-033-65)

Ingredients (1)

calcium carbonate (1000 mg/1)

Linked Drug Pages (1)

BERKLEY JENSEN ULTRA STRENGTH ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c7eedcbf-3b07-4cd3-937b-c56d7cc5bc57", "openfda": {"upc": ["0000000000000"], "unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["c7eedcbf-3b07-4cd3-937b-c56d7cc5bc57"], "manufacturer_name": ["BJWC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "265 TABLET, CHEWABLE in 1 BOTTLE (68391-033-65)", "package_ndc": "68391-033-65", "marketing_start_date": "20250317"}], "brand_name": "BERKLEY JENSEN ULTRA STRENGTH", "product_id": "68391-033_c7eedcbf-3b07-4cd3-937b-c56d7cc5bc57", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "68391-033", "generic_name": "ANTACID CALCIUM CARBONATE", "labeler_name": "BJWC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BERKLEY JENSEN", "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": "20250317", "listing_expiration_date": "20261231"}