Search by Drug Name or NDC
NDC 62135-0949-94 CYPROHEPTADINE 2 mg/5mL Details
CYPROHEPTADINE 2 mg/5mL
CYPROHEPTADINE is a ORAL SYRUP in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Chartwell RX, LLC. The primary component is CYPROHEPTADINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Cyproheptadine relieves red, irritated, itchy, watery eyes; sneezing; and runny nose caused by allergies, irritants in the air, and hay fever. It may also be used to relieve the itching of allergic skin conditions, and to treat hives, including hives caused by exposure to cold temperatures and by rubbing the skin. Cyproheptadine is also sometimes used to treat allergic reactions in people who have received blood products as part of medical treatment and to treat life-threatening allergic reactions after the symptoms have been brought under control with other medications. Cyproheptadine will help relieve symptoms but will not treat the cause of symptoms or speed recovery. Cyproheptadine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
Related Packages: 62135-0949-94Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Cyproheptadine
Product Information
| NDC | 62135-0949 |
|---|---|
| Product ID | 62135-949_06fd9a7b-3b04-6e0c-e063-6394a90aba46 |
| Associated GPIs | |
| GCN Sequence Number | 004010 |
| GCN Sequence Number Description | cyproheptadine HCl SYRUP 2 MG/5 ML ORAL |
| HIC3 | Z2P |
| HIC3 Description | ANTIHISTAMINES - 1ST GENERATION |
| GCN | 15803 |
| HICL Sequence Number | 001672 |
| HICL Sequence Number Description | CYPROHEPTADINE HCL |
| Brand/Generic | Generic |
| Proprietary Name | CYPROHEPTADINE |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | CYPROHEPTADINE HYDROCHLORIDE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | SYRUP |
| Route | ORAL |
| Active Ingredient Strength | 2 |
| Active Ingredient Units | mg/5mL |
| Substance Name | CYPROHEPTADINE HYDROCHLORIDE |
| Labeler Name | Chartwell RX, LLC |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA203191 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 62135-0949-94 (62135094994)
| NDC Package Code | 62135-949-94 |
|---|---|
| Billing NDC | 62135094994 |
| Package | 946 mL in 1 BOTTLE (62135-949-94) |
| Marketing Start Date | 2022-07-13 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |