NDC codes

FDA NDC Directory
Product NDC (as listed)70010-106Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70010-0106Add 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
70010-106-447001001064470010010644473 mL in 1 BOTTLE (70010-106-44)Marketed from Aug 19, 2025

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)
Glycopyrrolate Oral Solution
Generic name (nonproprietary)
glycopyrrolate
Active ingredients
Glycopyrrolate — 1 mg/5mL
Dosage form
Solution
Route
Oral
Labeler
Granules Pharmaceuticals Inc.NDC labeler code 70010
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214735
Marketing start
Listing expires
Other FDA classes
Cholinergic Antagonists (Mechanism)Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 70010-106_5d4ec411-0337-37ac-e063-6294a90a6b81SPL ID 5d4ec411-0337-37ac-e063-6294a90a6b81
Pharmacologic class
Anticholinergic; Cholinergic Muscarinic Antagonist

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

N470010010644 followed by a unit qualifier and the quantity

Package 70010-0106-44. 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 70010-106

What is NDC 70010-106?
70010-106 is the product NDC for Glycopyrrolate Oral Solution (glycopyrrolate), Glycopyrrolate 1 mg/5mL solution, listed with the FDA by Granules Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Glycopyrrolate Oral Solution (Glycopyrrolate).
What is the active ingredient?
Glycopyrrolate.
Who is the labeler?
Granules Pharmaceuticals Inc., NDC labeler code 70010. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Glycopyrrolate Oral Solution?
2 other product NDCs are listed under this name. See all Glycopyrrolate Oral Solution 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 Glycopyrrolate Oral Solution NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Glycopyrrolate Oral SolutionglycopyrrolateGlycopyrrolate 1 mg/5mLSolutionOralAJENAT PHARMACEUTICALS LLC82983-42882983-0428-47
Glycopyrrolate Oral SolutionGlycopyrrolate 1 mg/5mLLiquidOralSun Pharmaceutical Industries, Inc.51672-531651672-5316-09

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