Ala Scalp - 0316-0140-01 - (Hydrocortisone Acetate)

Alphabetical Index


Drug Information of Ala Scalp

Product NDC: 0316-0140
Proprietary Name: Ala Scalp
Non Proprietary Name: Hydrocortisone Acetate
Active Ingredient(s): 20    mg/mL & nbsp;   Hydrocortisone Acetate
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ala Scalp

Product NDC: 0316-0140
Labeler Name: Crown Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083231
Marketing Category: ANDA
Start Marketing Date: 19730228

Package Information of Ala Scalp

Package NDC: 0316-0140-01
Package Description: 29.6 mL in 1 BOTTLE, DROPPER (0316-0140-01)

NDC Information of Ala Scalp

NDC Code 0316-0140-01
Proprietary Name Ala Scalp
Package Description 29.6 mL in 1 BOTTLE, DROPPER (0316-0140-01)
Product NDC 0316-0140
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocortisone Acetate
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 19730228
Marketing Category Name ANDA
Labeler Name Crown Laboratories
Substance Name HYDROCORTISONE ACETATE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Ala Scalp


General Information