pregabalin

Generic: pregabalin

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pregabalin
Generic Name pregabalin
Labeler remedyrepack inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

pregabalin 225 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2980
Product ID 70518-2980_4abb620f-2f08-605d-e063-6394a90a9a7e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209743
DEA Schedule cv
Listing Expiration 2027-12-31
Marketing Start 2021-01-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182980
Hyphenated Format 70518-2980

Supplemental Identifiers

RxCUI
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
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2980-0)
source: ndc

Packages (1)

70518-2980-0 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2980-0)

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": "4abb620f-2f08-605d-e063-6394a90a9a7e", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["577127"], "spl_set_id": ["9111d695-9f3a-4b07-9daa-c1339b16acb3"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2980-0)", "package_ndc": "70518-2980-0", "marketing_start_date": "20210106"}], "brand_name": "Pregabalin", "product_id": "70518-2980_4abb620f-2f08-605d-e063-6394a90a9a7e", "dosage_form": "CAPSULE", "product_ndc": "70518-2980", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "REMEDYREPACK INC.", "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": "20210106", "listing_expiration_date": "20271231"}