pregabalin
Generic: pregabalin
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
pregabalin
Generic Name
pregabalin
Labeler
a-s medication solutions
Dosage Form
CAPSULE
Routes
Active Ingredients
pregabalin 75 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6793
Product ID
50090-6793_33934149-bafc-4450-978f-b141f6d0deed
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
500906793
Hyphenated Format
50090-6793
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
- 75 mg/1
Packaging
- 90 CAPSULE in 1 BOTTLE (50090-6793-0)
- 60 CAPSULE in 1 BOTTLE (50090-6793-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "33934149-bafc-4450-978f-b141f6d0deed", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483450"], "spl_set_id": ["54a9bfb4-dcff-491d-9676-1fe1d05e004c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-6793-0)", "package_ndc": "50090-6793-0", "marketing_start_date": "20231101"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (50090-6793-1)", "package_ndc": "50090-6793-1", "marketing_start_date": "20250509"}], "brand_name": "PREGABALIN", "product_id": "50090-6793_33934149-bafc-4450-978f-b141f6d0deed", "dosage_form": "CAPSULE", "product_ndc": "50090-6793", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREGABALIN", "active_ingredients": [{"name": "PREGABALIN", "strength": "75 mg/1"}], "application_number": "ANDA210432", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}