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 CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 100 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-148
Product ID 31722-148_2a2c08de-b06c-4926-e063-6394a90a2eb0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214956
Listing Expiration 2026-12-31
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 31722148
Hyphenated Format 31722-148

Supplemental Identifiers

RxCUI
310430 310431 310432
UPC
0331722148054
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 ANDA214956 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (31722-148-01)
  • 500 CAPSULE in 1 BOTTLE (31722-148-05)
  • 1000 CAPSULE in 1 BOTTLE (31722-148-10)
source: ndc

Packages (3)

Ingredients (1)

gabapentin (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a2c08de-b06c-4926-e063-6394a90a2eb0", "openfda": {"nui": ["N0000008486"], "upc": ["0331722148054"], "unii": ["6CW7F3G59X"], "rxcui": ["310430", "310431", "310432"], "spl_set_id": ["e8a30eb7-3fc5-456a-bdae-3f4095bf2c2b"], "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": "100 CAPSULE in 1 BOTTLE (31722-148-01)", "package_ndc": "31722-148-01", "marketing_start_date": "20210510"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (31722-148-05)", "package_ndc": "31722-148-05", "marketing_start_date": "20210510"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (31722-148-10)", "package_ndc": "31722-148-10", "marketing_start_date": "20210510"}], "brand_name": "GABAPENTIN", "product_id": "31722-148_2a2c08de-b06c-4926-e063-6394a90a2eb0", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "31722-148", "generic_name": "gabapentin", "labeler_name": "Camber Pharmaceuticals, Inc.", "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": "20261231"}