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NDC 50090-3148-00 Imipramine Hydrochloride 25 mg/1 Details
Imipramine Hydrochloride 25 mg/1
Imipramine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is IMIPRAMINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Imipramine tablets and capsules are used to treat depression. Imipramine tablets are also used to prevent bedwetting in children. Imipramine is in a class of medications called tricyclic antidepressants. It treats depression by increasing the amounts of certain natural substances in the brain that are needed to maintain mental balance. There is not enough information to explain how imipramine prevents bedwetting.
Related Packages: 50090-3148-00Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Imipramine
Product Information
| NDC | 50090-3148 |
|---|---|
| Product ID | 50090-3148_628d179c-a31b-4886-9f57-cb2c3fb32efd |
| Associated GPIs | 58200050100310 |
| GCN Sequence Number | 046069 |
| GCN Sequence Number Description | imipramine HCl TABLET 25 MG ORAL |
| HIC3 | H2U |
| HIC3 Description | TRICYCLIC ANTIDEPRESSANTS,REL.NON-SEL.REUPT-INHIB |
| GCN | 16542 |
| HICL Sequence Number | 001641 |
| HICL Sequence Number Description | IMIPRAMINE HCL |
| Brand/Generic | Generic |
| Proprietary Name | Imipramine Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Imipramine Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 25 |
| Active Ingredient Units | mg/1 |
| Substance Name | IMIPRAMINE HYDROCHLORIDE |
| Labeler Name | A-S Medication Solutions |
| Pharmaceutical Class | Tricyclic Antidepressant [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA040903 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50090-3148-00 (50090314800)
| NDC Package Code | 50090-3148-0 |
|---|---|
| Billing NDC | 50090314800 |
| Package | 30 TABLET, FILM COATED in 1 BOTTLE (50090-3148-0) |
| Marketing Start Date | 2017-10-03 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |