pregabalin

Generic: pregabalin

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pregabalin
Generic Name pregabalin
Labeler a-s medication solutions
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

pregabalin 200 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6504
Product ID 50090-6504_c157e81f-3496-4b3f-8b18-4919e67c3ec6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209357
DEA Schedule cv
Listing Expiration 2027-12-31
Marketing Start 2019-07-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906504
Hyphenated Format 50090-6504

Supplemental Identifiers

RxCUI
483446
UNII
55JG375S6M

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 ANDA209357 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 60 CAPSULE in 1 BOTTLE (50090-6504-0)
source: ndc

Packages (1)

50090-6504-0 60 CAPSULE in 1 BOTTLE (50090-6504-0)

Ingredients (1)

pregabalin (200 mg/1)

Linked Drug Pages (1)

Pregabalin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c157e81f-3496-4b3f-8b18-4919e67c3ec6", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483446"], "spl_set_id": ["5d33e9c7-6d81-485b-bf4a-9a588eda5208"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (50090-6504-0)", "package_ndc": "50090-6504-0", "marketing_start_date": "20230526"}], "brand_name": "Pregabalin", "product_id": "50090-6504_c157e81f-3496-4b3f-8b18-4919e67c3ec6", "dosage_form": "CAPSULE", "product_ndc": "50090-6504", "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": "200 mg/1"}], "application_number": "ANDA209357", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20271231"}