NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2042Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2042Add 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
72162-2042-27216220420272162204202473 mL in 1 BOTTLE, PLASTIC (72162-2042-2)Marketed from Mar 12, 2018

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
promethazine hydrochloride and codeine phosphate
Active ingredients
Promethazine hydrochloride — 6.25 mg/5mLCodeine phosphate — 10 mg/5mL
Dosage form
Solution
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 200386
Marketing start
Listing expires
DEA schedule
CV
Other FDA classes
Full Opioid Agonists (Mechanism)Phenothiazines (Chemical structure)
Identifiers
Product ID 72162-2042_14f5be0d-d8f8-4a3f-bfee-5d0a628361d7SPL ID 14f5be0d-d8f8-4a3f-bfee-5d0a628361d7SPL set ID df2c24ba-1c88-4ec3-b2a1-801358ec645cRxCUI 991486UNII R61ZEH7I1I, GSL05Y1MN6
Pharmacologic class
Opioid Agonist; Phenothiazine

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

N472162204202 followed by a unit qualifier and the quantity

Package 72162-2042-02. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Promethazine HCl and Codeine Phosphate Oral Solution is indicated for the temporary relief of coughs and upper respiratory symptoms associated with allergy or the common cold in patients 18 years of age and older. Important Limitations of Use Not indicated for pediatric patients under 18 years of age [ see Use in Specific Populations (8.4) ]. Contraindicated in pediatric patients under 12 years of age [ see Contraindications (4) , Use in Specific Populations (8.4) ]. Contraindicated in pediatric patients 12 to 18 years of age after tonsillectomy or adenoidectomy [ see Contraindications (4) , Use in Specific Populations (8.4) ]. Because of the risks of addiction, abuse, and misuse with opioid…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2042

What is NDC 72162-2042?
72162-2042 is the product NDC for Promethazine Hydrochloride and Codeine Phosphate, Promethazine hydrochloride 6.25 mg/5mL; Codeine phosphate 10 mg/5mL solution, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Promethazine Hydrochloride and Codeine Phosphate.
What is the active ingredient?
Promethazine hydrochloride, Codeine phosphate.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Promethazine Hydrochloride and Codeine Phosphate?
4 other product NDCs are listed under this name. See all Promethazine Hydrochloride and Codeine Phosphate 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 Promethazine Hydrochloride and Codeine Phosphate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Promethazine Hydrochloride and Codeine PhosphatePromethazine hydrochloride 6.25 mg/5mL; Codeine phosphate 10 mg/5mLSolutionOralCosette Pharmaceuticals, Inc.0713-082300713-0823-75
Promethazine Hydrochloride and Codeine PhosphatePromethazine hydrochloride 6.25 mg/5mL; Codeine phosphate 10 mg/5mLSolutionOralQUAGEN PHARMACEUTICALS LLC70752-13970752-0139-0670752-0139-12
Promethazine Hydrochloride and Codeine PhosphatePromethazine hydrochloride 6.25 mg/5mL; Codeine phosphate 10 mg/5mLSolutionOralATLANTIC BIOLOGICALS CORP.17856-006517856-0065-0117856-0065-02
Promethazine Hydrochloride and Codeine PhosphatePromethazine hydrochloride 6.25 mg/5mL; Codeine phosphate 10 mg/5mLSolutionOralCranbury Pharmaceuticals, LLC27808-06527808-0065-02

Other NDCs under ANDA 200386

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

FDA NDC Directory listings under ANDA 200386
ProductStrengthForm · routeLabelerProduct NDC
Promethazine Hydrochloride and Codeine PhosphatePromethazine hydrochloride 6.25 mg/5mL; Codeine phosphate 10 mg/5mLSolutionOralCosette Pharmaceuticals, Inc.0713-0823
Promethazine Hydrochloride and Codeine PhosphatePromethazine hydrochloride 6.25 mg/5mL; Codeine phosphate 10 mg/5mLSolutionOralATLANTIC BIOLOGICALS CORP.17856-0065
Promethazine Hydrochloride and Codeine PhosphatePromethazine hydrochloride 6.25 mg/5mL; Codeine phosphate 10 mg/5mLSolutionOralCranbury Pharmaceuticals, LLC27808-065

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