pregabalin
Generic: pregabalin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
pregabalin
Generic Name
pregabalin
Labeler
bryant ranch prepack
Dosage Form
CAPSULE
Routes
Active Ingredients
pregabalin 150 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2304
Product ID
72162-2304_250c155b-3d38-41f9-945b-e983a206e583
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210432
DEA Schedule
cv
Listing Expiration
2026-12-31
Marketing Start
2019-07-19
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622304
Hyphenated Format
72162-2304
Supplemental Identifiers
RxCUI
UNII
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
pregabalin (source: ndc)
Generic Name
pregabalin (source: ndc)
Application Number
ANDA210432 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 150 mg/1
Packaging
- 1000 CAPSULE in 1 BOTTLE (72162-2304-0)
- 90 CAPSULE in 1 BOTTLE (72162-2304-9)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "250c155b-3d38-41f9-945b-e983a206e583", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483440"], "spl_set_id": ["335e3bcb-10a3-481b-ad95-ee9ceaa3689e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (72162-2304-0)", "package_ndc": "72162-2304-0", "marketing_start_date": "20240430"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72162-2304-9)", "package_ndc": "72162-2304-9", "marketing_start_date": "20240430"}], "brand_name": "PREGABALIN", "product_id": "72162-2304_250c155b-3d38-41f9-945b-e983a206e583", "dosage_form": "CAPSULE", "product_ndc": "72162-2304", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREGABALIN", "active_ingredients": [{"name": "PREGABALIN", "strength": "150 mg/1"}], "application_number": "ANDA210432", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}