Ranitidine Hydrochloride

Product NDC

42291-736

11-digit product format

422910736

Labeler code

42291

Product ID

42291-736_8634d978-d166-2bb3-e053-2a91aa0a77cf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA075742

Marketing category

ANDA

Marketing start

2017-03-31

Marketing end

0000-00-00

Substance

RANITIDINE HYDROCHLORIDE

Active strength

300 mg/1

Pharmacologic classes

Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record