Package 71656-017-04

Brand: metformin hydrochloride oral solution

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71656-017-04
Digits Only 7165601704
Product NDC 71656-017
Product ID 71656-017_29f72dd3-74fc-29f4-e063-6294a90a4755
Description

118 mL in 1 BOTTLE (71656-017-04)

Marketing

Marketing Status
Marketed Since 2024-07-31
Brand metformin hydrochloride oral solution
Generic metformin hydrochloride
Sample Package No

Linked Drug Pages (1)

Metformin Hydrochloride Oral Solution ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "29f72dd3-74fc-29f4-e063-6294a90a4755", "openfda": {"upc": ["0371656017040"], "unii": ["786Z46389E"], "rxcui": ["861025"], "spl_set_id": ["df61d56e-18ff-404c-b671-42b39aa23574"], "manufacturer_name": ["Saptalis Pharmaceuticals, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (71656-017-04)", "package_ndc": "71656-017-04", "marketing_start_date": "20240731"}], "brand_name": "Metformin Hydrochloride Oral Solution", "product_id": "71656-017_29f72dd3-74fc-29f4-e063-6294a90a4755", "dosage_form": "SOLUTION", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "71656-017", "generic_name": "Metformin Hydrochloride", "labeler_name": "Saptalis Pharmaceuticals, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride Oral Solution", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/5mL"}], "application_number": "ANDA211309", "marketing_category": "ANDA", "marketing_start_date": "20240731", "listing_expiration_date": "20261231"}