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NDC 69842-0869-62 Acid Reducer 150 mg/1 Details
Acid Reducer 150 mg/1
Acid Reducer is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by CVS HEALTH CORP. The primary component is RANITIDINE HYDROCHLORIDE.
Product Information
| NDC | 69842-0869 |
|---|---|
| Product ID | 69842-869_bacda134-86bb-85b2-6559-07560c8feccf |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Acid Reducer |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Ranitidine |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, COATED |
| Route | ORAL |
| Active Ingredient Strength | 150 |
| Active Ingredient Units | mg/1 |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Labeler Name | CVS HEALTH CORP |
| Pharmaceutical Class | Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA078192 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 69842-0869-62 (69842086962)
| NDC Package Code | 69842-869-62 |
|---|---|
| Billing NDC | 69842086962 |
| Package | 1 BOTTLE in 1 CARTON (69842-869-62) / 95 TABLET, COATED in 1 BOTTLE |
| Marketing Start Date | 2010-05-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |