Clindamycin Phosphate NDC 68462-866

NDC codes

FDA NDC Directory

Product NDC (as listed)68462-866Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68462-0866Add 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
68462-866-35	68462086635	1 TUBE in 1 CARTON (68462-866-35) / 30 g in 1 TUBEMarketed from Feb 10, 2021
68462-866-65	68462086665	1 TUBE in 1 CARTON (68462-866-65) / 60 g in 1 TUBEMarketed from Feb 10, 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): Clindamycin Phosphate
Generic name (nonproprietary): clindamycin phosphate
Active ingredients: Clindamycin phosphate — 10 mg/g
Dosage form: Gel
Route: Topical
Labeler: GLENMARK PHARMACEUTICALS INC., USA
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 214251
Marketing start: Feb 10, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Decreased Sebaceous Gland Activity (Physiologic effect)Lincosamides (Chemical structure)Neuromuscular Blockade (Physiologic effect)
Identifiers: Product ID 68462-866_a914f752-12b0-41d3-9ec6-0095f9b87859SPL ID a914f752-12b0-41d3-9ec6-0095f9b87859SPL set ID d36bad26-f337-4a71-a6e5-d97b60f4e385RxCUI 2676585UNII EH6D7113I8UPC 0368462866351
Pharmacologic class: Lincosamide Antibacterial

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468462086635 followed by a unit qualifier and the quantity

Package 68462-0866-35. 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 Jan 28, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Clindamycin phosphate gel is indicated in the treatment of acne vulgaris. In view of the potential for diarrhea, bloody diarrhea and pseudomembranous colitis, the physician should consider whether other agents are more appropriate (see CONTRAINDICATIONS , WARNINGS and ADVERSE REACTIONS ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 214251

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

FDA NDC Directory listings under ANDA 214251
Product	Strength	Form · route	Labeler	Product NDC
Clindamycin Phosphate	Clindamycin phosphate 10 mg/g	GelTopical	NORTHSTAR RX LLC	16714-161
Clindamycin Phosphate	Clindamycin phosphate 10 mg/g	GelTopical	A-S Medication Solutions	50090-6072