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BF-PARADAC
BF-PARADAC - 10884-2228-2 - (Acetaminophen)
Drug Information of BF-PARADAC
| Product NDC: | 10884-2228 |
| Proprietary Name: | BF-PARADAC |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 500 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BF-PARADAC
| Product NDC: | 10884-2228 |
| Labeler Name: | Bright Future Pharmaceuticals Factory |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20010916 |
Package Information of BF-PARADAC
| Package NDC: | 10884-2228-2 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (10884-2228-2) > 10 TABLET in 1 BLISTER PACK (10884-2228-1) |
NDC Information of BF-PARADAC
| NDC Code | 10884-2228-2 |
| Proprietary Name | BF-PARADAC |
| Package Description | 2 BLISTER PACK in 1 CARTON (10884-2228-2) > 10 TABLET in 1 BLISTER PACK (10884-2228-1) |
| Product NDC | 10884-2228 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010916 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Bright Future Pharmaceuticals Factory |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
