Pilocarpine Hydrochloride NDC 63629-8351

NDC codes

FDA NDC Directory

Product NDC (as listed)63629-8351Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63629-8351Add 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
63629-8351-1	63629835101	30 TABLET, FILM COATED in 1 BOTTLE (63629-8351-1)Marketed from Sep 2, 2020

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

Brand name (proprietary): Pilocarpine Hydrochloride
Generic name (nonproprietary): pilocarpine hydrochloride
Active ingredients: Pilocarpine hydrochloride — 5 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Bryant Ranch Prepack
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077220
Marketing start: Oct 14, 2005
Listing expires: Dec 31, 2026
Other FDA classes: Cholinergic Agonists (Mechanism)Cholinergic Muscarinic Agonists (Mechanism)
Identifiers: Product ID 63629-8351_be3bf41c-ed8c-420a-a9c4-72e3e9e1c869SPL ID be3bf41c-ed8c-420a-a9c4-72e3e9e1c869SPL set ID fb97323d-acec-4e4a-af16-efef66d969dcRxCUI 1000913UNII 0WW6D218XJ
Pharmacologic class: Cholinergic Receptor 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

N463629835101 followed by a unit qualifier and the quantity

Package 63629-8351-01. 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 077220

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

FDA NDC Directory listings under ANDA 077220
Product	Strength	Form · route	Labeler	Product NDC
Pilocarpine Hydrochloride	Pilocarpine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	Lannett Company, Inc.	0527-1407
Pilocarpine Hydrochloride	Pilocarpine hydrochloride 5 mg/1	Tablet, Film coatedOral	AvPAK	50268-652
Pilocarpine Hydrochloride	Pilocarpine hydrochloride 5 mg/1	Tablet, Film coatedOral	Lannett Company, Inc.	0527-1313
Pilocarpine Hydrochloride	Pilocarpine hydrochloride 5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-1078
Pilocarpine Hydrochloride	Pilocarpine hydrochloride 5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-2099