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NDC 70010-0228-05 Gabapentin 800 mg/1 Details
Gabapentin 800 mg/1
Gabapentin is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Granules Pharmaceuticals Inc.. The primary component is GABAPENTIN.
Product Information
| NDC | 70010-0228 |
|---|---|
| Product ID | 70010-228_fc5cd0f5-29ce-00c3-e053-6394a90aac29 |
| Associated GPIs | |
| GCN Sequence Number | 041806 |
| GCN Sequence Number Description | gabapentin TABLET 800 MG ORAL |
| HIC3 | H4B |
| HIC3 Description | ANTICONVULSANTS |
| GCN | 94447 |
| HICL Sequence Number | 008831 |
| HICL Sequence Number Description | GABAPENTIN |
| Brand/Generic | Generic |
| Proprietary Name | Gabapentin |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Gabapentin |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 800 |
| Active Ingredient Units | mg/1 |
| Substance Name | GABAPENTIN |
| Labeler Name | Granules Pharmaceuticals Inc. |
| Pharmaceutical Class | Decreased Central Nervous System Disorganized Electrical Activity [PE] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA217116 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70010-0228-05 (70010022805)
| NDC Package Code | 70010-228-05 |
|---|---|
| Billing NDC | 70010022805 |
| Package | 500 TABLET, FILM COATED in 1 BOTTLE (70010-228-05) |
| Marketing Start Date | 2023-06-27 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |