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Atopalm Maximum Strength Anti-Itch
Atopalm Maximum Strength Anti-Itch - 51141-6010-1 - (HYDROCORTISONE)
Drug Information of Atopalm Maximum Strength Anti-Itch
| Product NDC: | 51141-6010 |
| Proprietary Name: | Atopalm Maximum Strength Anti-Itch |
| Non Proprietary Name: | HYDROCORTISONE |
| Active Ingredient(s): | 1 g/100g & nbsp; HYDROCORTISONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Atopalm Maximum Strength Anti-Itch
| Product NDC: | 51141-6010 |
| Labeler Name: | NeoPharm Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111104 |
Package Information of Atopalm Maximum Strength Anti-Itch
| Package NDC: | 51141-6010-1 |
| Package Description: | 1 TUBE in 1 CARTON (51141-6010-1) > 28.3 g in 1 TUBE |
NDC Information of Atopalm Maximum Strength Anti-Itch
| NDC Code | 51141-6010-1 |
| Proprietary Name | Atopalm Maximum Strength Anti-Itch |
| Package Description | 1 TUBE in 1 CARTON (51141-6010-1) > 28.3 g in 1 TUBE |
| Product NDC | 51141-6010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROCORTISONE |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20111104 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | NeoPharm Co., Ltd. |
| Substance Name | HYDROCORTISONE |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
