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BudPak Anti-Itch
BudPak Anti-Itch - 27293-017-01 - (Hydrocortisone)
Drug Information of BudPak Anti-Itch
| Product NDC: | 27293-017 |
| Proprietary Name: | BudPak Anti-Itch |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | .01 g/g & nbsp; Hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BudPak Anti-Itch
| Product NDC: | 27293-017 |
| Labeler Name: | Budpak Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121217 |
Package Information of BudPak Anti-Itch
| Package NDC: | 27293-017-01 |
| Package Description: | 1 TUBE in 1 BOX (27293-017-01) > 14 g in 1 TUBE (27293-017-14) |
NDC Information of BudPak Anti-Itch
| NDC Code | 27293-017-01 |
| Proprietary Name | BudPak Anti-Itch |
| Package Description | 1 TUBE in 1 BOX (27293-017-01) > 14 g in 1 TUBE (27293-017-14) |
| Product NDC | 27293-017 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20121217 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Budpak Inc. |
| Substance Name | HYDROCORTISONE |
| Strength Number | .01 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
