pregabalin

Generic: pregabalin

Labeler: preferred pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pregabalin
Generic Name pregabalin
Labeler preferred pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

pregabalin 50 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-7521
Product ID 68788-7521_7f697241-584d-4ef6-8018-35d302908108
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208677
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 687887521
Hyphenated Format 68788-7521

Supplemental Identifiers

RxCUI
483448
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 ANDA208677 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (68788-7521-1)
  • 30 CAPSULE in 1 BOTTLE (68788-7521-3)
  • 60 CAPSULE in 1 BOTTLE (68788-7521-6)
  • 90 CAPSULE in 1 BOTTLE (68788-7521-9)
source: ndc

Packages (4)

Ingredients (1)

pregabalin (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7f697241-584d-4ef6-8018-35d302908108", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483448"], "spl_set_id": ["3dbfd868-8408-4514-ba1c-04a5d095c16a"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68788-7521-1)", "package_ndc": "68788-7521-1", "marketing_start_date": "20191028"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68788-7521-3)", "package_ndc": "68788-7521-3", "marketing_start_date": "20191028"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (68788-7521-6)", "package_ndc": "68788-7521-6", "marketing_start_date": "20191028"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (68788-7521-9)", "package_ndc": "68788-7521-9", "marketing_start_date": "20191028"}], "brand_name": "Pregabalin", "product_id": "68788-7521_7f697241-584d-4ef6-8018-35d302908108", "dosage_form": "CAPSULE", "product_ndc": "68788-7521", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "50 mg/1"}], "application_number": "ANDA208677", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}