What is NDC 55111-799?

55111-799 is the product NDC for Guaifenesin and Pseudoephedrine HCL, Guaifenesin 1200 mg/1; Pseudoephedrine hydrochloride 120 mg/1 tablet, extended release, listed with the FDA by Dr. Reddy's Laboratories Limited. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Guaifenesin, Pseudoephedrine hydrochloride.

Dr. Reddy's Laboratories Limited, NDC labeler code 55111. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Guaifenesin and Pseudoephedrine HCL?

14 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Guaifenesin and Pseudoephedrine HCL NDC 55111-799

Unfinished product

This listing is a drug for further processing, not a finished drug product dispensed or administered to patients. It is not normally billed.

NDC codes

FDA NDC Directory

Product NDC (as listed)55111-799Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55111-0799Add 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
55111-799-84	5511107998455111079984	5 BLISTER PACK in 1 CARTON (55111-799-84) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from 29-DEC-17

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

Generic name (nonproprietary): guaifenesin and pseudoephedrine hcl
Active ingredients: Guaifenesin — 1200 mg/1Pseudoephedrine hydrochloride — 120 mg/1
Dosage form: Tablet, Extended release
Labeler: Dr. Reddy's Laboratories LimitedNDC labeler code 55111
Product type: Drug for further processing
Marketing category: Drug for further processing
Marketing start: Dec 29, 2017
Listing expires: Dec 31, 2027
Identifiers: Product ID 55111-799_5850587b-d311-8b8f-a16e-6a0aef29b0ddSPL ID 5850587b-d311-8b8f-a16e-6a0aef29b0dd

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N455111079984 followed by a unit qualifier and the quantity

Package 55111-0799-84. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 55111-799

What is NDC 55111-799?: 55111-799 is the product NDC for Guaifenesin and Pseudoephedrine HCL, Guaifenesin 1200 mg/1; Pseudoephedrine hydrochloride 120 mg/1 tablet, extended release, listed with the FDA by Dr. Reddy's Laboratories Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Guaifenesin and Pseudoephedrine HCL.
What is the active ingredient?: Guaifenesin, Pseudoephedrine hydrochloride.
Who is the labeler?: Dr. Reddy's Laboratories Limited, NDC labeler code 55111. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Guaifenesin and Pseudoephedrine HCL?: 14 other product NDCs are listed under this name. See all Guaifenesin and Pseudoephedrine HCL NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Guaifenesin and Pseudoephedrine HCL NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Guaifenesin and Pseudoephedrine HCl	Guaifenesin 600 mg/1; Pseudoephedrine hydrochloride 60 mg/1	Tablet, Extended releaseOral	Strategic Sourcing Services LLC	70677-1263	70677-1263-01
Guaifenesin and Pseudoephedrine HCl	Guaifenesin 600 mg/1; Pseudoephedrine hydrochloride 60 mg/1	Tablet, Extended releaseOral	Amerisource Bergen	46122-801	46122-0801-08
Guaifenesin and Pseudoephedrine HCl	Guaifenesin 600 mg/1; Pseudoephedrine hydrochloride 60 mg/1	Tablet, Extended releaseOral	Granules India Ltd	62207-827	62207-0827-72
Guaifenesin and Pseudoephedrine HCl	Guaifenesin 1200 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	Granules India Ltd	62207-828	62207-0828-71
Guaifenesin and Pseudoephedrine HCl	Guaifenesin 600 mg/1; Pseudoephedrine hydrochloride 60 mg/1	Tablet, Extended releaseOral	WALGREEN CO.	0363-9946	00363-9946-4000363-9946-45
Guaifenesin and Pseudoephedrine HCl	Guaifenesin 600 mg/1; Pseudoephedrine hydrochloride 60 mg/1	Tablet, Extended releaseOral	Rite Aid Corporation	11822-0046	11822-0046-0111822-0046-02
Guaifenesin and Pseudoephedrine HCl	Guaifenesin 600 mg/1; Pseudoephedrine hydrochloride 60 mg/1	Tablet, Extended releaseOral	Meijer	79481-1002	79481-1002-01
Guaifenesin and Pseudoephedrine HCl	Guaifenesin 600 mg/1; Pseudoephedrine hydrochloride 60 mg/1	Tablet, Extended releaseOral	KROGER COMPANY	30142-137	30142-0137-1230142-0137-17
Guaifenesin and Pseudoephedrine HCl	Guaifenesin 600 mg/1; Pseudoephedrine hydrochloride 60 mg/1	Tablet, Extended releaseOral	Ohm Laboratories, Inc.	51660-074	51660-0074-18
Guaifenesin and Pseudoephedrine HCl	Guaifenesin 1200 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Extended releaseOral	Ohm Laboratories, Inc.	51660-077	51660-0077-12

All 15 Guaifenesin and Pseudoephedrine HCL NDCs

NDC codes

Product information

Billing references

Product label

About NDC 55111-799

Related NDCs: other Guaifenesin and Pseudoephedrine HCL products