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NDC 72789-0178-82 Primidone 50 mg/1 Details
Primidone 50 mg/1
Primidone is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is PRIMIDONE.
MedlinePlus Drug Summary
Primidone is used alone or with other medications to control certain types of seizures. Primidone is in a class of medications called anticonvulsants. It works by decreasing abnormal electrical activity in the brain.
Related Packages: 72789-0178-82Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Primidone
Product Information
| NDC | 72789-0178 |
|---|---|
| Product ID | 72789-178_0e76f0d9-0ac0-e097-e063-6394a90adba2 |
| Associated GPIs | 72600060000305 |
| GCN Sequence Number | 004544 |
| GCN Sequence Number Description | primidone TABLET 50 MG ORAL |
| HIC3 | H4B |
| HIC3 Description | ANTICONVULSANTS |
| GCN | 17322 |
| HICL Sequence Number | 001886 |
| HICL Sequence Number Description | PRIMIDONE |
| Brand/Generic | Generic |
| Proprietary Name | Primidone |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Primidone |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/1 |
| Substance Name | PRIMIDONE |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Pharmaceutical Class | Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA040586 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 72789-0178-82 (72789017882)
| NDC Package Code | 72789-178-82 |
|---|---|
| Billing NDC | 72789017882 |
| Package | 500 TABLET in 1 BOTTLE, PLASTIC (72789-178-82) |
| Marketing Start Date | 2021-06-22 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |