Acid Reducer Powder NDC 75907-237

NDC codes

FDA NDC Directory

Product NDC (as listed)75907-237Labeler and product segments. Claims need a package NDC.

Product NDC at billing width75907-0237Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
75907-237-14	75907023714	14 PACKET in 1 CARTON (75907-237-14) / 1 POWDER, FOR SUSPENSION in 1 PACKETMarketed from Dec 15, 2024
75907-237-42	75907023742	42 PACKET in 1 CARTON (75907-237-42) / 1 POWDER, FOR SUSPENSION in 1 PACKETMarketed from Mar 3, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Acid Reducer Powder
Generic name (nonproprietary): omeprazole and sodium bicarbonate
Active ingredients: Omeprazole — 20 mg/1Sodium bicarbonate — 1680 mg/1
Dosage form: Powder, For suspension
Route: Oral
Labeler: Dr. Reddy's Laboratories Inc.,
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217784
Marketing start: Jul 15, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Alkalinizing Activity (Mechanism)Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
Identifiers: Product ID 75907-237_46176916-f5b6-7f16-2601-3885bca7659fSPL ID 46176916-f5b6-7f16-2601-3885bca7659fSPL set ID 6f8452f8-8c2c-6700-a11d-1531023056c5RxCUI 753562UNII KG60484QX9, 8MDF5V39QO
Pharmacologic class: Proton Pump Inhibitor

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N475907023714 followed by a unit qualifier and the quantity

Package 75907-0237-14. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Mar 3, 2025.

Indications (excerpt from the label)

Use(s) treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn. This drug may take 1 to 4 days for full effect.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 217784

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 217784
Product	Strength	Form · route	Labeler	Product NDC
Omeprazole and Sodium Bicarbonate	Omeprazole 20 mg/1; Sodium bicarbonate 1680 mg/1	Powder, For suspensionOral	Dr. Reddy's Laboratories Inc.,	43598-010
Omeprazole and Sodium Bicarbonate	Omeprazole 20 mg/1; Sodium bicarbonate 1680 mg/1	Powder, For suspensionOral	Dr. Reddy's Laboratories Inc.,	75907-138
Omeprazole and Sodium Bicarbonate	Omeprazole 20 mg/1; Sodium bicarbonate 1680 mg/1	Powder, For suspensionOral	Dr. Reddy's Laboratories Inc.,	43598-307