Ascorbic Acid

Product NDC

69877-017

11-digit product format

698770017

Labeler code

69877

Product ID

69877-017_491facd5-ead0-3a7f-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ascorbic Acid

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS

Labeler

Raw Materials International Overseas LLC

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2015-07-02

Marketing end

0000-00-00

Substance

ASCORBIC ACID

Active strength

500 mg/mL

Pharmacologic classes

Vitamin C [EPC],Ascorbic Acid [CS]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record