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Diphenoxylate Hydrochloride and Atropine Sulfate

Approved
Approval ID

7a7ff864-f4e4-48da-94c2-6ccbc30de49c

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

May 24, 2011

Manufacturers
FDA

RedPharm Drug, Inc.

DUNS: 008039641

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

diphenoxylate hydrochloride and atropine sulfate

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code67296-0505
Application NumberANDA085762
Product Classification
M
Marketing Category
C73584
G
Generic Name
diphenoxylate hydrochloride and atropine sulfate
Product Specifications
Route of AdministrationORAL
Effective DateMay 23, 2011
FDA Product Classification

INGREDIENTS (6)

SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
ATROPINE SULFATEActive
Quantity: .025 mg in 1 1
Code: 03J5ZE7KA5
Classification: ACTIB
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
DIPHENOXYLATE HYDROCHLORIDEActive
Quantity: 2.5 mg in 1 1
Code: W24OD7YW48
Classification: ACTIB

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Diphenoxylate Hydrochloride and Atropine Sulfate - FDA Drug Approval Details