gabapentin
Generic: gabapentin
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
gabapentin
Generic Name
gabapentin
Labeler
a-s medication solutions
Dosage Form
CAPSULE
Routes
Active Ingredients
gabapentin 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-0949
Product ID
50090-0949_bf9abed3-bc5b-4606-831d-1ae78cdea91d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078787
Listing Expiration
2026-12-31
Marketing Start
2008-01-31
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500900949
Hyphenated Format
50090-0949
Supplemental Identifiers
RxCUI
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
ANDA078787 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (50090-0949-0)
- 100 CAPSULE in 1 BOTTLE (50090-0949-1)
- 90 CAPSULE in 1 BOTTLE (50090-0949-2)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bf9abed3-bc5b-4606-831d-1ae78cdea91d", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["ecb798a0-377d-4712-bb82-ec9d7116962f"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-0949-0)", "package_ndc": "50090-0949-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (50090-0949-1)", "package_ndc": "50090-0949-1", "marketing_start_date": "20141128"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-0949-2)", "package_ndc": "50090-0949-2", "marketing_start_date": "20141128"}], "brand_name": "Gabapentin", "product_id": "50090-0949_bf9abed3-bc5b-4606-831d-1ae78cdea91d", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-0949", "generic_name": "Gabapentin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA078787", "marketing_category": "ANDA", "marketing_start_date": "20080131", "listing_expiration_date": "20261231"}