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Analpram Advanced
Analpram Advanced - 0496-0731-64 - (hydrocortisone acetate and pramoxine hydrochloride)
Drug Information of Analpram Advanced
| Product NDC: | 0496-0731 |
| Proprietary Name: | Analpram Advanced |
| 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 Advanced
| Product NDC: | 0496-0731 |
| Labeler Name: | Ferndale Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101001 |
Package Information of Analpram Advanced
| Package NDC: | 0496-0731-64 |
| Package Description: | 1 KIT in 1 CARTON (0496-0731-64) * 30 TUBE, WITH APPLICATOR in 1 CARTON (0496-0799-64) > 4 g in 1 TUBE, WITH APPLICATOR (0496-0799-36) * 30 PACKET in 1 CARTON > .025 g in 1 PACKET |
NDC Information of Analpram Advanced
| NDC Code | 0496-0731-64 |
| Proprietary Name | Analpram Advanced |
| Package Description | 1 KIT in 1 CARTON (0496-0731-64) * 30 TUBE, WITH APPLICATOR in 1 CARTON (0496-0799-64) > 4 g in 1 TUBE, WITH APPLICATOR (0496-0799-36) * 30 PACKET in 1 CARTON > .025 g in 1 PACKET |
| Product NDC | 0496-0731 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocortisone acetate and pramoxine hydrochloride |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20101001 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Ferndale Laboratories, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
