gabapentin
Generic: gabapentin
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
gabapentin
Generic Name
gabapentin
Labeler
nucare pharmaceuticals,inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
gabapentin 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-5017
Product ID
68071-5017_1b4081b8-badf-b16e-e063-6294a90a1cab
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090007
Listing Expiration
2026-12-31
Marketing Start
2015-12-30
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680715017
Hyphenated Format
68071-5017
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
gabapentin (source: ndc)
Generic Name
gabapentin (source: ndc)
Application Number
ANDA090007 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (68071-5017-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b4081b8-badf-b16e-e063-6294a90a1cab", "openfda": {"nui": ["N0000008486"], "upc": ["0368071501711"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["8f785189-bf66-36cc-e053-2a95a90a7cbc"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68071-5017-1)", "package_ndc": "68071-5017-1", "marketing_start_date": "20190806"}], "brand_name": "GABAPENTIN", "product_id": "68071-5017_1b4081b8-badf-b16e-e063-6294a90a1cab", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68071-5017", "generic_name": "GABAPENTIN", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA090007", "marketing_category": "ANDA", "marketing_start_date": "20151230", "listing_expiration_date": "20261231"}