pregabalin

Generic: pregabalin

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pregabalin
Generic Name pregabalin
Labeler direct_rx
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

pregabalin 225 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-045
Product ID 72189-045_2be8eb66-533f-0815-e063-6294a90a115d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209743
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2020-12-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189045
Hyphenated Format 72189-045

Supplemental Identifiers

RxCUI
483438 483442 483444 483446 577127
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 ANDA209743 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 225 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (72189-045-30)
  • 60 CAPSULE in 1 BOTTLE (72189-045-60)
  • 90 CAPSULE in 1 BOTTLE (72189-045-90)
source: ndc

Packages (3)

72189-045-30 30 CAPSULE in 1 BOTTLE (72189-045-30) 72189-045-60 60 CAPSULE in 1 BOTTLE (72189-045-60) 72189-045-90 90 CAPSULE in 1 BOTTLE (72189-045-90)

Ingredients (1)

pregabalin (225 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": "2be8eb66-533f-0815-e063-6294a90a115d", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483438", "483442", "483444", "483446", "577127"], "spl_set_id": ["91cf12b1-e1a6-dbc2-e053-2a95a90a8d5d"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-045-30)", "package_ndc": "72189-045-30", "marketing_start_date": "20201201"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (72189-045-60)", "package_ndc": "72189-045-60", "marketing_start_date": "20201201"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72189-045-90)", "package_ndc": "72189-045-90", "marketing_start_date": "20201201"}], "brand_name": "PREGABALIN", "product_id": "72189-045_2be8eb66-533f-0815-e063-6294a90a115d", "dosage_form": "CAPSULE", "product_ndc": "72189-045", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREGABALIN", "active_ingredients": [{"name": "PREGABALIN", "strength": "225 mg/1"}], "application_number": "ANDA209743", "marketing_category": "ANDA", "marketing_start_date": "20201201", "listing_expiration_date": "20261231"}