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Sunmark acid reducer
Sunmark acid reducer - 49348-733-44 - (Ranitidine)
Drug Information of Sunmark acid reducer
| Product NDC: | 49348-733 |
| Proprietary Name: | Sunmark acid reducer |
| Non Proprietary Name: | Ranitidine |
| Active Ingredient(s): | 75 mg/1 & nbsp; Ranitidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunmark acid reducer
| Product NDC: | 49348-733 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076760 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090710 |
Package Information of Sunmark acid reducer
| Package NDC: | 49348-733-44 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-733-44) > 30 TABLET in 1 BOTTLE |
NDC Information of Sunmark acid reducer
| NDC Code | 49348-733-44 |
| Proprietary Name | Sunmark acid reducer |
| Package Description | 1 BOTTLE in 1 CARTON (49348-733-44) > 30 TABLET in 1 BOTTLE |
| Product NDC | 49348-733 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ranitidine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090710 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Strength Number | 75 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
