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
68071-3664
Product ID
68071-3664_2eaeb82e-d306-5079-e063-6294a90a33d1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214956
Listing Expiration
2026-12-31
Marketing Start
2021-05-10
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713664
Hyphenated Format
68071-3664
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
ANDA214956 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (68071-3664-3)
- 40 CAPSULE in 1 BOTTLE (68071-3664-4)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2eaeb82e-d306-5079-e063-6294a90a33d1", "openfda": {"nui": ["N0000008486"], "upc": ["0368071366440"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["200b61d7-6e4c-923d-e063-6294a90a42cf"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68071-3664-3)", "package_ndc": "68071-3664-3", "marketing_start_date": "20250221"}, {"sample": false, "description": "40 CAPSULE in 1 BOTTLE (68071-3664-4)", "package_ndc": "68071-3664-4", "marketing_start_date": "20210510"}], "brand_name": "GABAPENTIN", "product_id": "68071-3664_2eaeb82e-d306-5079-e063-6294a90a33d1", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68071-3664", "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": "ANDA214956", "marketing_category": "ANDA", "marketing_start_date": "20210510", "listing_expiration_date": "20261231"}