Analpram HC is a Topical Cream in the Human Prescription Drug category. It is labeled and distributed by Sebela Pharmaceuticals Inc.. The primary component is Hydrocortisone Acetate; Pramoxine Hydrochloride.
Product ID | 54766-799_35f8330a-aae3-13d3-e054-00144ff8d46c |
NDC | 54766-799 |
Product Type | Human Prescription Drug |
Proprietary Name | Analpram HC |
Generic Name | Hydrocortisone Acetate And Pramoxine Hydrochloride |
Dosage Form | Cream |
Route of Administration | TOPICAL |
Marketing Start Date | 2015-08-07 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | Sebela Pharmaceuticals Inc. |
Substance Name | HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE |
Active Ingredient Strength | 25 mg/g; mg/g |
Pharm Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2015-08-07 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | GM |
Marketing Start Date | 2015-08-07 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | GM |
Marketing Start Date | 2015-08-07 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-08-07 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | GM |
Marketing Start Date | 2015-08-07 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-08-07 |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | GM |
Marketing Start Date | 2015-08-07 |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-08-07 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
HYDROCORTISONE ACETATE | 25 mg/g |
SPL SET ID: | fecf8380-3bb5-11e5-98c5-0002a5d5c51b |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
54766-778 | Analpram HC | hydrocortisone acetate and pramoxine hydrochloride |
54766-799 | Analpram HC | hydrocortisone acetate and pramoxine hydrochloride |
54766-829 | Analpram HC | hydrocortisone acetate and pramoxine hydrochloride |
71399-2501 | hydrocortisone acetate and pramoxine hydrochloride | hydrocortisone acetate and pramoxine hydrochloride |
69367-285 | Hydrocortisone Acetate Pramoxine Hydrochloride | Hydrocortisone Acetate and Pramoxine Hydrochloride |
73028-401 | Hydrocortisone Acetate Pramoxine Hydrochloride | Hydrocortisone Acetate and Pramoxine Hydrochloride |
79043-240 | Hydrocortisone Acetate Pramoxine Hydrochloride | HYDROCORTISONE ACETATE and PRAMOXINE HYDROCHLORIDE |
69646-704 | Novacort | hydrocortisone acetate and pramoxine hydrochloride |
49908-150 | PRAMCORT | HYDROCORTISONE ACETATE and PRAMOXINE HYDROCHLORIDE |
54766-726 | Pramosone | hydrocortisone acetate and pramoxine hydrochloride |
54766-729 | Pramosone | hydrocortisone acetate and pramoxine hydrochloride |
54766-760 | Pramosone | hydrocortisone acetate and pramoxine hydrochloride |
54766-763 | pramosone | hydrocortisone acetate and pramoxine hydrochloride |
54766-777 | Pramosone | hydrocortisone acetate and pramoxine hydrochloride |
54766-716 | Pramosone Cream | hydrocortisone acetate and pramoxine hydrochloride |
21695-982 | Proctofoam | hydrocortisone acetate and pramoxine hydrochloride |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ANALPRAM HC 73659750 1476501 Live/Registered |
FERNDALE LABORATORIES, INC. 1987-05-08 |