70518-2351 NDC - IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	70518-2351-0	6 POUCH in 1 CARTON (70518-2351-0) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL

Field Name	Field Value	Definition
PRODUCT NDC	70518-2351	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	Ipratropium Bromide and Albuterol Sulfate	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
START MARKETING DATE	10/7/2019	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
END MARKETING DATE	3/31/2021	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
MARKETING CATEGORY NAME	ANDA	The translation of the dosage form Code submitted by the firm.
APPLICATION NUMBER	ANDA077559	The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAME	REMEDYREPACK INC.	Name of Company corresponding to the labeler code segment of the Product NDC.