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Penicillin V Potassium
Penicillin V Potassium - 21695-318-40 - (Penicillin V Potassium)
Drug Information of Penicillin V Potassium
| Product NDC: | 21695-318 |
| Proprietary Name: | Penicillin V Potassium |
| Non Proprietary Name: | Penicillin V Potassium |
| Active Ingredient(s): | 500 mg/1 & nbsp; Penicillin V Potassium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Penicillin V Potassium
| Product NDC: | 21695-318 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062935 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19881123 |
Package Information of Penicillin V Potassium
| Package NDC: | 21695-318-40 |
| Package Description: | 40 TABLET in 1 BOTTLE (21695-318-40) |
NDC Information of Penicillin V Potassium
| NDC Code | 21695-318-40 |
| Proprietary Name | Penicillin V Potassium |
| Package Description | 40 TABLET in 1 BOTTLE (21695-318-40) |
| Product NDC | 21695-318 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Penicillin V Potassium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19881123 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | PENICILLIN V POTASSIUM |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
