gabapentin

Generic: gabapentin

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler a-s medication solutions
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 100 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7388
Product ID 50090-7388_71191297-6f1b-48d3-a1c6-a5bcbeb18f0f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214956
Listing Expiration 2027-12-31
Marketing Start 2021-05-10

Pharmacologic Class

Physiologic Effect
decreased central nervous system disorganized electrical activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907388
Hyphenated Format 50090-7388

Supplemental Identifiers

RxCUI
310430
UNII
6CW7F3G59X
NUI
N0000008486

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (50090-7388-0)
  • 100 CAPSULE in 1 BOTTLE (50090-7388-1)
  • 90 CAPSULE in 1 BOTTLE (50090-7388-2)
  • 42 CAPSULE in 1 BOTTLE (50090-7388-3)
source: ndc

Packages (4)

50090-7388-0 30 CAPSULE in 1 BOTTLE (50090-7388-0) 50090-7388-1 100 CAPSULE in 1 BOTTLE (50090-7388-1) 50090-7388-2 90 CAPSULE in 1 BOTTLE (50090-7388-2) 50090-7388-3 42 CAPSULE in 1 BOTTLE (50090-7388-3)

Ingredients (1)

gabapentin (100 mg/1)

Linked Drug Pages (1)

GABAPENTIN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "71191297-6f1b-48d3-a1c6-a5bcbeb18f0f", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["7ea0b220-edbb-45eb-aeb3-65283f8489a1"], "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 (50090-7388-0)", "package_ndc": "50090-7388-0", "marketing_start_date": "20241021"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (50090-7388-1)", "package_ndc": "50090-7388-1", "marketing_start_date": "20241021"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-7388-2)", "package_ndc": "50090-7388-2", "marketing_start_date": "20241021"}, {"sample": false, "description": "42 CAPSULE in 1 BOTTLE (50090-7388-3)", "package_ndc": "50090-7388-3", "marketing_start_date": "20241021"}], "brand_name": "GABAPENTIN", "product_id": "50090-7388_71191297-6f1b-48d3-a1c6-a5bcbeb18f0f", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7388", "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": "ANDA214956", "marketing_category": "ANDA", "marketing_start_date": "20210510", "listing_expiration_date": "20271231"}