gabapentin
Generic: gabapentin
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
gabapentin
Generic Name
gabapentin
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
gabapentin 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-289
Product ID
72789-289_4badb0d6-c979-2f30-e063-6294a90a1e7d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204989
Listing Expiration
2027-12-31
Marketing Start
2016-02-18
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789289
Hyphenated Format
72789-289
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
ANDA204989 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-289-30)
- 60 CAPSULE in 1 BOTTLE, PLASTIC (72789-289-60)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4badb0d6-c979-2f30-e063-6294a90a1e7d", "openfda": {"nui": ["N0000008486"], "upc": ["0372789289304"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["4a95f18e-0de4-4ce1-9f97-bc2e8a5bac6a"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (72789-289-30)", "package_ndc": "72789-289-30", "marketing_start_date": "20221205"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE, PLASTIC (72789-289-60)", "package_ndc": "72789-289-60", "marketing_start_date": "20250529"}], "brand_name": "Gabapentin", "product_id": "72789-289_4badb0d6-c979-2f30-e063-6294a90a1e7d", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72789-289", "generic_name": "Gabapentin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA204989", "marketing_category": "ANDA", "marketing_start_date": "20160218", "listing_expiration_date": "20271231"}