NDC codes

FDA NDC Directory
Product NDC (as listed)51316-993Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51316-0993Add 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 NDC11-digit (billing)PackageCopy
51316-993-18513160993181 BLISTER PACK in 1 CARTON (51316-993-18) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from May 6, 2021
51316-993-36513160993362 BLISTER PACK in 1 CARTON (51316-993-36) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from May 6, 2021

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)
Guaifenesin D
Generic name (nonproprietary)
guaifenesin and pseudoephedrine hydrochloride
Active ingredients
Guaifenesin — 600 mg/1Pseudoephedrine hydrochloride — 60 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212542
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Agonists (Mechanism)Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Respiratory Secretions (Physiologic effect)
Identifiers
Product ID 51316-993_85bd100e-7bbc-4ab0-9f19-e119a28f16d3SPL ID 85bd100e-7bbc-4ab0-9f19-e119a28f16d3SPL set ID 4dee850b-b170-4ef9-ae02-3db9bfa05abeRxCUI 1305603UNII 495W7451VQ, 6V9V2RYJ8N
Pharmacologic class
Expectorant; alpha-Adrenergic Agonist

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

N451316099318 followed by a unit qualifier and the quantity

Package 51316-0993-18. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 212542

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

FDA NDC Directory listings under ANDA 212542
ProductStrengthForm · routeLabelerProduct NDC
Guaifenesin and Pseudoephedrine HClGuaifenesin 600 mg/1; Pseudoephedrine hydrochloride 60 mg/1Tablet, Extended releaseOralOhm Laboratories, Inc.51660-074
Guaifenesin and Pseudoephedrine HClGuaifenesin 1200 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Extended releaseOralOhm Laboratories, Inc.51660-077
Guaifenesin Dguaifenesin and pseudoephedrine hydrochlorideGuaifenesin 600 mg/1; Pseudoephedrine hydrochloride 60 mg/1Tablet, Extended releaseOralRUGBY LABORATORIES, INC.0536-1333
Guaifenesin Dguaifenesin and pseudoephedrine hydrochlorideGuaifenesin 600 mg/1; Pseudoephedrine hydrochloride 60 mg/1Tablet, Extended releaseOralWalgreen Company0363-9930
Guaifenesin and Pseudoephedrine HydrochlorideGuaifenesin 600 mg/1; Pseudoephedrine hydrochloride 60 mg/1Tablet, Extended releaseOralSTRATEGIC SOURCING SERVICES LLC62011-0475
Guaifenesin and Pseudoephedrine HClGuaifenesin 600 mg/1; Pseudoephedrine hydrochloride 60 mg/1Tablet, Extended releaseOralStrategic Sourcing Services LLC70677-1263
MAXIMUM STRENGTH Mucus Dguaifenesin and pseudoephedrine hydrochlorideGuaifenesin 1200 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Extended releaseOralCVS Pharmacy51316-970
Guaifenesin and Pseudoephedrine HydrochlorideGuaifenesin 600 mg/1; Pseudoephedrine hydrochloride 60 mg/1Tablet, Extended releaseOralPUBLIX SUPER MARKETS, INC41415-994

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