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NDC 72789-0139-01 Buspirone Hydrochloride 5 mg/1 Details
Buspirone Hydrochloride 5 mg/1
Buspirone Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is BUSPIRONE HYDROCHLORIDE.
MedlinePlus Drug Summary
Buspirone is used to treat anxiety disorders or in the short-term treatment of symptoms of anxiety. Buspirone is in a class of medications called anxiolytics. It works by changing the amounts of certain natural substances in the brain.
Related Packages: 72789-0139-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Buspirone
Product Information
| NDC | 72789-0139 |
|---|---|
| Product ID | 72789-139_0bdc5a82-2d09-04d9-e063-6294a90a625a |
| Associated GPIs | 57200005100310 |
| GCN Sequence Number | 003782 |
| GCN Sequence Number Description | buspirone HCl TABLET 5 MG ORAL |
| HIC3 | H2F |
| HIC3 Description | ANTI-ANXIETY DRUGS |
| GCN | 28890 |
| HICL Sequence Number | 001620 |
| HICL Sequence Number Description | BUSPIRONE HCL |
| Brand/Generic | Generic |
| Proprietary Name | Buspirone Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | buspirone hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 5 |
| Active Ingredient Units | mg/1 |
| Substance Name | BUSPIRONE HYDROCHLORIDE |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA075388 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 72789-0139-01 (72789013901)
| NDC Package Code | 72789-139-01 |
|---|---|
| Billing NDC | 72789013901 |
| Package | 100 TABLET in 1 BOTTLE, PLASTIC (72789-139-01) |
| Marketing Start Date | 2020-11-06 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |