lanthanum carbonate
Generic: lanthanum carbonate
Labeler: ascend laboratories, llcDrug Facts
Product Profile
Brand Name
lanthanum carbonate
Generic Name
lanthanum carbonate
Labeler
ascend laboratories, llc
Dosage Form
TABLET, CHEWABLE
Routes
Active Ingredients
lanthanum carbonate 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67877-256
Product ID
67877-256_ba371296-8731-4ffa-ab36-aff022e48d52
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202329
Listing Expiration
2026-12-31
Marketing Start
2025-05-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67877256
Hyphenated Format
67877-256
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
lanthanum carbonate (source: ndc)
Generic Name
lanthanum carbonate (source: ndc)
Application Number
ANDA202329 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 2 BOTTLE in 1 CARTON (67877-256-90) / 45 TABLET, CHEWABLE in 1 BOTTLE (67877-256-45)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ba371296-8731-4ffa-ab36-aff022e48d52", "openfda": {"upc": ["0367877256900", "0367877256450", "0367877258119", "0367877257150"], "unii": ["490D9F069T"], "rxcui": ["477347", "602635", "642452"], "spl_set_id": ["22b07167-2b7b-42ba-9ae9-cf58c98a2ab2"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BOTTLE in 1 CARTON (67877-256-90) / 45 TABLET, CHEWABLE in 1 BOTTLE (67877-256-45)", "package_ndc": "67877-256-90", "marketing_start_date": "20250510"}], "brand_name": "Lanthanum Carbonate", "product_id": "67877-256_ba371296-8731-4ffa-ab36-aff022e48d52", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "67877-256", "generic_name": "Lanthanum Carbonate", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lanthanum Carbonate", "active_ingredients": [{"name": "LANTHANUM CARBONATE", "strength": "500 mg/1"}], "application_number": "ANDA202329", "marketing_category": "ANDA", "marketing_start_date": "20250510", "listing_expiration_date": "20261231"}