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NDC 43598-0808-65 Ranitidine 150 mg/1 Details
Ranitidine 150 mg/1
Ranitidine is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Dr. Reddy's Laboratories Inc.. The primary component is RANITIDINE HYDROCHLORIDE.
Product Information
| NDC | 43598-0808 |
|---|---|
| Product ID | 43598-808_f6dfcff2-d313-5722-171d-8d4d5af59951 |
| 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, COATED |
| Route | ORAL |
| Active Ingredient Strength | 150 |
| Active Ingredient Units | mg/1 |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Labeler Name | Dr. Reddy's Laboratories Inc. |
| 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 43598-0808-65 (43598080865)
| NDC Package Code | 43598-808-65 |
|---|---|
| Billing NDC | 43598080865 |
| Package | 1 BOTTLE in 1 CARTON (43598-808-65) / 220 TABLET, COATED in 1 BOTTLE |
| Marketing Start Date | 2018-12-26 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |