Ranitidine Hydrochloride

Product NDC

42291-767

11-digit product format

422910767

Labeler code

42291

Product ID

42291-767_8efc060e-5c6f-645a-e053-2995a90a7197

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

AvKARE, Inc

Application

ANDA211893

Marketing category

ANDA

Marketing start

2019-08-19

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