Acetaminophen And Codeine

Product NDC

68788-9259

11-digit product format

687889259

Labeler code

68788

Product ID

68788-9259_3e9c2bd7-bdfa-43c8-acc9-c11cea938b1d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

acetaminophen and codeine phosphate

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA089828

Marketing category

ANDA

Marketing start

2014-11-13

Marketing end

0000-00-00

Substance

CODEINE PHOSPHATE; ACETAMINOPHEN

Active strength

60 mg/1; mg/1

Pharmacologic classes

Full Opioid Agonists [MoA],Opioid Agonist [EPC]

DEA schedule

CIII

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record