pregabalin

Generic: pregabalin

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

Drug Facts

Product Profile

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

pregabalin 75 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-121
Product ID 62332-121_1e87ec6d-6f2d-400f-bf21-08fcce28bb6c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203459
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 62332121
Hyphenated Format 62332-121

Supplemental Identifiers

RxCUI
483438 483440 483442 483444 483446 483448 483450 577127
UPC
0362332124305 0362332122301 0362332125302 0362332126309 0362332123308
UNII
55JG375S6M

Packaging Origin

Original Packager
true

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 ANDA203459 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 CARTON (62332-121-10)
  • 30 CAPSULE in 1 BOTTLE (62332-121-30)
  • 90 CAPSULE in 1 BOTTLE (62332-121-90)
  • 1000 CAPSULE in 1 BOTTLE (62332-121-91)
source: ndc

Packages (4)

Ingredients (1)

pregabalin (75 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1e87ec6d-6f2d-400f-bf21-08fcce28bb6c", "openfda": {"upc": ["0362332124305", "0362332122301", "0362332125302", "0362332126309", "0362332123308"], "unii": ["55JG375S6M"], "rxcui": ["483438", "483440", "483442", "483444", "483446", "483448", "483450", "577127"], "spl_set_id": ["cf7b4b67-b017-47ac-af3f-bde5bd07bb0c"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 CARTON (62332-121-10)", "package_ndc": "62332-121-10", "marketing_start_date": "20190719"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (62332-121-30)", "package_ndc": "62332-121-30", "marketing_start_date": "20190719"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (62332-121-90)", "package_ndc": "62332-121-90", "marketing_start_date": "20190719"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (62332-121-91)", "package_ndc": "62332-121-91", "marketing_start_date": "20190719"}], "brand_name": "Pregabalin", "product_id": "62332-121_1e87ec6d-6f2d-400f-bf21-08fcce28bb6c", "dosage_form": "CAPSULE", "product_ndc": "62332-121", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "75 mg/1"}], "application_number": "ANDA203459", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}