pregabalin

Generic: pregabalin

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pregabalin
Generic Name pregabalin
Labeler asclemed usa, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

pregabalin 150 mg/1

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-121
Product ID 76420-121_a8e4e23f-490f-7ebc-e053-2a95a90af171
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 76420121
Hyphenated Format 76420-121

Supplemental Identifiers

RxCUI
483438 483440 483442 483444 483446 483448 483450 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 ANDA210432 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (76420-121-30)
  • 60 CAPSULE in 1 BOTTLE (76420-121-60)
  • 90 CAPSULE in 1 BOTTLE (76420-121-90)
source: ndc

Packages (3)

Ingredients (1)

pregabalin (150 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a8e4e23f-490f-7ebc-e053-2a95a90af171", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483438", "483440", "483442", "483444", "483446", "483448", "483450", "577127"], "spl_set_id": ["69b8a843-a3a8-4d76-8418-f48288625030"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (76420-121-30)", "package_ndc": "76420-121-30", "marketing_start_date": "20200625"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (76420-121-60)", "package_ndc": "76420-121-60", "marketing_start_date": "20200625"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (76420-121-90)", "package_ndc": "76420-121-90", "marketing_start_date": "20200625"}], "brand_name": "PREGABALIN", "product_id": "76420-121_a8e4e23f-490f-7ebc-e053-2a95a90af171", "dosage_form": "CAPSULE", "product_ndc": "76420-121", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREGABALIN", "active_ingredients": [{"name": "PREGABALIN", "strength": "150 mg/1"}], "application_number": "ANDA210432", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}