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NDC 63868-0482-60 Ranitidine 75 mg/1 Details
Ranitidine 75 mg/1
Ranitidine is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Chain Drug Marketing Association. The primary component is RANITIDINE HYDROCHLORIDE.
Product Information
| NDC | 63868-0482 |
|---|---|
| Product ID | 63868-482_d5a0c763-85d7-7813-a6a7-fbec0176b522 |
| 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 | Ranitidine |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Ranitidine |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 75 |
| Active Ingredient Units | mg/1 |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Labeler Name | Chain Drug Marketing Association |
| Pharmaceutical Class | Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA075294 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 63868-0482-60 (63868048260)
| NDC Package Code | 63868-482-60 |
|---|---|
| Billing NDC | 63868048260 |
| Package | 1 BOTTLE in 1 CARTON (63868-482-60) / 60 TABLET in 1 BOTTLE |
| Marketing Start Date | 2018-07-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |