pioglitazone and metformin hydrochloride
Generic: pioglitazone and metformin hydrochloride
Labeler: macleods pharmaceuticals limitedDrug Facts
Product Profile
Brand Name
pioglitazone and metformin hydrochloride
Generic Name
pioglitazone and metformin hydrochloride
Labeler
macleods pharmaceuticals limited
Dosage Form
TABLET
Routes
Active Ingredients
metformin hydrochloride 850 mg/1, pioglitazone hydrochloride 15 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
33342-177
Product ID
33342-177_c05a0d40-cee7-4a54-90e5-acd59e23f8f3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204802
Listing Expiration
2026-12-31
Marketing Start
2015-11-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
33342177
Hyphenated Format
33342-177
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
pioglitazone and metformin hydrochloride (source: ndc)
Generic Name
pioglitazone and metformin hydrochloride (source: ndc)
Application Number
ANDA204802 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 850 mg/1
- 15 mg/1
Packaging
- 60 TABLET in 1 BOTTLE (33342-177-09)
- 100 TABLET in 1 BOTTLE (33342-177-11)
- 10 BLISTER PACK in 1 CARTON (33342-177-12) / 10 TABLET in 1 BLISTER PACK
- 1000 TABLET in 1 BOTTLE (33342-177-44)
- 180 TABLET in 1 BOTTLE (33342-177-57)
Packages (5)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c05a0d40-cee7-4a54-90e5-acd59e23f8f3", "openfda": {"upc": ["0333342177117", "0333342177094", "0333342176448"], "unii": ["JQT35NPK6C", "786Z46389E"], "rxcui": ["861783", "861822"], "spl_set_id": ["5ff2cd9e-a579-48f5-845f-c37a68372a34"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (33342-177-09)", "package_ndc": "33342-177-09", "marketing_start_date": "20151106"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (33342-177-11)", "package_ndc": "33342-177-11", "marketing_start_date": "20151106"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-177-12) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "33342-177-12", "marketing_start_date": "20151106"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (33342-177-44)", "package_ndc": "33342-177-44", "marketing_start_date": "20151106"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (33342-177-57)", "package_ndc": "33342-177-57", "marketing_start_date": "20151106"}], "brand_name": "Pioglitazone and metformin hydrochloride", "product_id": "33342-177_c05a0d40-cee7-4a54-90e5-acd59e23f8f3", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]", "Peroxisome Proliferator Receptor alpha Agonist [EPC]", "Peroxisome Proliferator Receptor gamma Agonist [EPC]", "Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]", "Peroxisome Proliferator-activated Receptor gamma Agonists [MoA]", "Thiazolidinedione [EPC]", "Thiazolidinediones [CS]"], "product_ndc": "33342-177", "generic_name": "Pioglitazone and metformin hydrochloride", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pioglitazone and metformin hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "850 mg/1"}, {"name": "PIOGLITAZONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA204802", "marketing_category": "ANDA", "marketing_start_date": "20151106", "listing_expiration_date": "20261231"}