Alendronate sodium tablet

CHEBI:CHEBI_747701

Drug Classification

Important Medical Information

⚕️ This information is sourced from ChEBI (Chemical Entities of Biological Interest) database and is intended for educational purposes only.

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Additional Identifiers

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Additional Attributes

brand_name
Alendronate
brand_name_base
Alendronate
rxcui
904431
product_type
HUMAN PRESCRIPTION DRUG
listing_expiration_date
20251231
route
ORAL
dosage_form
TABLET
marketing_category
ANDA
active_ingredient_strength
70 mg/1
marketing_start_date
20201201
package_marketing_start_date
20201201
active_ingredient_name
ALENDRONATE SODIUM
generic_name
Alendronate sodium tablet
product_ndc
10135-719
application_number
ANDA090258
labeler_name
Marlex Pharmaceuticals, Inc.
manufacturer_name
Marlex Pharmaceuticals, Inc.
spl_id
22042768-7f67-4a80-e063-6394a90ab089
package_ndc
10135-719-44
package_description
1 BLISTER PACK in 1 CARTON (10135-719-44) / 4 TABLET in 1 BLISTER PACK
unii
2UY4M2U3RA
spl_set_id
b63421af-ec03-1de7-e053-2a95a90abec6
pharm_class
Diphosphonates [CS]
22-rdf-syntax-ns#type
http://www.w3.org/2002/07/owl#Class