pregabalin

Generic: pregabalin

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

Drug Facts

Product Profile

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

pregabalin 75 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-612
Product ID 31722-612_3ff00691-3fde-ae93-e063-6294a90adcc5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206912
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2019-10-08

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722612
Hyphenated Format 31722-612

Supplemental Identifiers

RxCUI
483438 483440 483442 483444 483446 483448 483450 577127
UPC
0331722615907 0331722613903 0331722614900 0331722611909 0331722610902 0331722617901 0331722616904 0331722612906
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 ANDA206912 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 500 CAPSULE in 1 BOTTLE (31722-612-05)
  • 10 BLISTER PACK in 1 CARTON (31722-612-31) / 10 CAPSULE in 1 BLISTER PACK
  • 60 CAPSULE in 1 BOTTLE (31722-612-60)
  • 90 CAPSULE in 1 BOTTLE (31722-612-90)
source: ndc

Packages (4)

31722-612-05 500 CAPSULE in 1 BOTTLE (31722-612-05) 31722-612-31 10 BLISTER PACK in 1 CARTON (31722-612-31) / 10 CAPSULE in 1 BLISTER PACK 31722-612-60 60 CAPSULE in 1 BOTTLE (31722-612-60) 31722-612-90 90 CAPSULE in 1 BOTTLE (31722-612-90)

Ingredients (1)

pregabalin (75 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": "3ff00691-3fde-ae93-e063-6294a90adcc5", "openfda": {"upc": ["0331722615907", "0331722613903", "0331722614900", "0331722611909", "0331722610902", "0331722617901", "0331722616904", "0331722612906"], "unii": ["55JG375S6M"], "rxcui": ["483438", "483440", "483442", "483444", "483446", "483448", "483450", "577127"], "spl_set_id": ["241c4b7e-f719-4828-8639-ea613b8a6583"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (31722-612-05)", "package_ndc": "31722-612-05", "marketing_start_date": "20191008"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-612-31)  / 10 CAPSULE in 1 BLISTER PACK", "package_ndc": "31722-612-31", "marketing_start_date": "20191008"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (31722-612-60)", "package_ndc": "31722-612-60", "marketing_start_date": "20191008"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (31722-612-90)", "package_ndc": "31722-612-90", "marketing_start_date": "20191008"}], "brand_name": "Pregabalin", "product_id": "31722-612_3ff00691-3fde-ae93-e063-6294a90adcc5", "dosage_form": "CAPSULE", "product_ndc": "31722-612", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "75 mg/1"}], "application_number": "ANDA206912", "marketing_category": "ANDA", "marketing_start_date": "20191008", "listing_expiration_date": "20261231"}