gabapentin

Generic: gabapentin

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

gabapentin 600 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2842
Product ID 70518-2842_4ab769da-4554-e9a5-e063-6294a90a767d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206402
Listing Expiration 2027-12-31
Marketing Start 2020-08-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182842
Hyphenated Format 70518-2842

Supplemental Identifiers

RxCUI
310433
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 ANDA206402 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 POUCH in 1 BOX (70518-2842-1) / 1 TABLET in 1 POUCH (70518-2842-2)
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-2842-3)
source: ndc

Packages (2)

70518-2842-1 100 POUCH in 1 BOX (70518-2842-1) / 1 TABLET in 1 POUCH (70518-2842-2) 70518-2842-3 90 TABLET in 1 BOTTLE, PLASTIC (70518-2842-3)

Ingredients (1)

gabapentin (600 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": "4ab769da-4554-e9a5-e063-6294a90a767d", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["81243958-cc5a-4ec0-a64d-71682f949d5f"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2842-1)  / 1 TABLET in 1 POUCH (70518-2842-2)", "package_ndc": "70518-2842-1", "marketing_start_date": "20210805"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-2842-3)", "package_ndc": "70518-2842-3", "marketing_start_date": "20251103"}], "brand_name": "Gabapentin", "product_id": "70518-2842_4ab769da-4554-e9a5-e063-6294a90a767d", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-2842", "generic_name": "Gabapentin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA206402", "marketing_category": "ANDA", "marketing_start_date": "20200820", "listing_expiration_date": "20271231"}