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Analpram E
Analpram E - 0496-0750-33 - (Hydrocortisone Acetate and Pramoxine Hydrochloride)
Drug Information of Analpram E
| Product NDC: | 0496-0750 |
| Proprietary Name: | Analpram E |
| Non Proprietary Name: | Hydrocortisone Acetate and Pramoxine Hydrochloride |
| Active Ingredient(s): | & nbsp; Hydrocortisone Acetate and Pramoxine Hydrochloride |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Analpram E
| Product NDC: | 0496-0750 |
| Labeler Name: | Ferndale Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 20090901 |
Package Information of Analpram E
| Package NDC: | 0496-0750-33 |
| Package Description: | 1 KIT in 1 CARTON (0496-0750-33) * 4 g in 1 TUBE, WITH APPLICATOR (0496-0755-33) * 6 g in 1 POUCH (0496-0749-76) |
NDC Information of Analpram E
| NDC Code | 0496-0750-33 |
| Proprietary Name | Analpram E |
| Package Description | 1 KIT in 1 CARTON (0496-0750-33) * 4 g in 1 TUBE, WITH APPLICATOR (0496-0755-33) * 6 g in 1 POUCH (0496-0749-76) |
| Product NDC | 0496-0750 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone Acetate and Pramoxine Hydrochloride |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20090901 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | Ferndale Laboratories, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
