Ascorbic Acid Injection
FDA Label NDC 70771-1943

1 label section · Submitted to the FDA by Zydus Lifesciences Limited · Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zydus Lifesciences Limited for the product Ascorbic Acid (NDC 70771-1943). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Package Label.Principal Display Panel

Ascorbic Acid Injection, USP

2,500 mg/5 mL (500 mg/mL)

NDC 70771-1943-1

Rx Only

2500 mg Label (Db495704 Ebb9 4090 B28a B30b73e10ffa 01)

2500 mg Label (Db495704 Ebb9 4090 B28a B30b73e10ffa 01)

Ascorbic Acid Injection, USP

5,000 mg/10 mL (500 mg/mL)

NDC 70771-1944-1

Rx Only

5000 mg Label (Db495704 Ebb9 4090 B28a B30b73e10ffa 02)

5000 mg Label (Db495704 Ebb9 4090 B28a B30b73e10ffa 02)

Ascorbic Acid Injection, USP

25,000 mg/50 mL (500 mg/mL)

NDC 70771-1945-1

Rx Only

25000 mg Label (Db495704 Ebb9 4090 B28a B30b73e10ffa 03)

25000 mg Label (Db495704 Ebb9 4090 B28a B30b73e10ffa 03)

* Please review the disclaimer below.