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AMOXICILLIN
AMOXICILLIN - 43598-219-01 - (amoxicillin)
Drug Information of AMOXICILLIN
| Product NDC: | 43598-219 |
| Proprietary Name: | AMOXICILLIN |
| Non Proprietary Name: | amoxicillin |
| Active Ingredient(s): | 875 mg/1 & nbsp; amoxicillin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AMOXICILLIN
| Product NDC: | 43598-219 |
| Labeler Name: | Dr Reddys Laboratories Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050754 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19780710 |
Package Information of AMOXICILLIN
| Package NDC: | 43598-219-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (43598-219-01) |
NDC Information of AMOXICILLIN
| NDC Code | 43598-219-01 |
| Proprietary Name | AMOXICILLIN |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (43598-219-01) |
| Product NDC | 43598-219 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | amoxicillin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19780710 |
| Marketing Category Name | NDA |
| Labeler Name | Dr Reddys Laboratories Inc |
| Substance Name | AMOXICILLIN |
| Strength Number | 875 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
