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NDC 70934-0238-30 MECLIZINE HYDROCHLORIDE 25 mg/1 Details
MECLIZINE HYDROCHLORIDE 25 mg/1
MECLIZINE HYDROCHLORIDE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. dba Northwind Pharmaceuticals. The primary component is MECLIZINE HYDROCHLORIDE.
Product Information
| NDC | 70934-0238 |
|---|---|
| Product ID | 70934-238_f1ee8cb0-32d0-a9a9-e053-2a95a90a1061 |
| Associated GPIs | 50200050000310 |
| GCN Sequence Number | 004732 |
| GCN Sequence Number Description | meclizine HCl TABLET 25 MG ORAL |
| HIC3 | H6J |
| HIC3 Description | ANTIEMETIC/ANTIVERTIGO AGENTS |
| GCN | 18302 |
| HICL Sequence Number | 001975 |
| HICL Sequence Number Description | MECLIZINE HCL |
| Brand/Generic | Generic |
| Proprietary Name | MECLIZINE HYDROCHLORIDE |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Meclizine Hydrocloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 25 |
| Active Ingredient Units | mg/1 |
| Substance Name | MECLIZINE HYDROCHLORIDE |
| Labeler Name | Denton Pharma, Inc. dba Northwind Pharmaceuticals |
| Pharmaceutical Class | Antiemetic [EPC], Emesis Suppression [PE] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA040659 |
| Listing Certified Through | n/a |
Package
NDC 70934-0238-30 (70934023830)
| NDC Package Code | 70934-238-30 |
|---|---|
| Billing NDC | 70934023830 |
| Package | 30 TABLET in 1 BOTTLE, PLASTIC (70934-238-30) |
| Marketing Start Date | 2019-01-09 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |