gabapentin

Generic: gabapentin

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler camber pharmaceuticals, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

gabapentin 250 mg/5mL

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-069
Product ID 31722-069_45c076af-c121-6962-e063-6394a90aaad1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217682
Listing Expiration 2026-12-31
Marketing Start 2024-01-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722069
Hyphenated Format 31722-069

Supplemental Identifiers

RxCUI
283523
UPC
0331722069472
UNII
6CW7F3G59X
NUI
N0000008486

Packaging Origin

Original Packager
true

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 ANDA217682 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (31722-069-47) / 470 mL in 1 BOTTLE
source: ndc

Packages (1)

31722-069-47 1 BOTTLE in 1 CARTON (31722-069-47) / 470 mL in 1 BOTTLE

Ingredients (1)

gabapentin (250 mg/5mL)

Linked Drug Pages (1)

GABAPENTIN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45c076af-c121-6962-e063-6394a90aaad1", "openfda": {"nui": ["N0000008486"], "upc": ["0331722069472"], "unii": ["6CW7F3G59X"], "rxcui": ["283523"], "spl_set_id": ["b86c81d9-9a4a-4847-be18-520e5cc5dc4b"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (31722-069-47)  / 470 mL in 1 BOTTLE", "package_ndc": "31722-069-47", "marketing_start_date": "20240117"}], "brand_name": "GABAPENTIN", "product_id": "31722-069_45c076af-c121-6962-e063-6394a90aaad1", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "31722-069", "generic_name": "GABAPENTIN", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "250 mg/5mL"}], "application_number": "ANDA217682", "marketing_category": "ANDA", "marketing_start_date": "20240117", "listing_expiration_date": "20261231"}