NDC codes

FDA NDC Directory
Product NDC (as listed)70010-907Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70010-0907Add 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
70010-907-017001009070170010090701100 CAPSULE in 1 BOTTLE (70010-907-01)Marketed from Dec 21, 2020

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)
Penicillamine
Generic name (nonproprietary)
penicillamine
Active ingredients
Penicillamine — 250 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Granules Pharmaceuticals Inc.NDC labeler code 70010
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211735
Marketing start
Listing expires
Identifiers
Product ID 70010-907_5d4f1d8a-c945-db1b-e063-6394a90a68fbSPL ID 5d4f1d8a-c945-db1b-e063-6394a90a68fb
Pharmacologic class
Antirheumatic Agent

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

N470010090701 followed by a unit qualifier and the quantity

Package 70010-0907-01. 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

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

About NDC 70010-907

What is NDC 70010-907?
70010-907 is the product NDC for Penicillamine, Penicillamine 250 mg/1 capsule, 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?
Penicillamine.
What is the active ingredient?
Penicillamine.
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 Penicillamine?
8 other product NDCs are listed under this name. See all Penicillamine 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 Penicillamine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
PenicillaminePenicillamine 250 mg/1CapsuleOralNavinta LLC68475-20168475-0201-01
PenicillaminePenicillamine 250 mg/1CapsuleOralBreckenridge Pharmaceutical, Inc.51991-97451991-0974-01
PenicillaminePenicillamine 250 mg/1TabletOralLupin Pharmaceuticals, Inc.70748-15370748-0153-01
PenicillaminePenicillamine 250 mg/1CapsuleOralProficient Rx LP71205-91671205-0916-00
PenicillaminePenicillamine 250 mg/1Capsule, Gelatin coatedOralDr. Reddy's Laboratories Inc.43598-63443598-0634-01
PenicillaminePenicillamine 250 mg/1CapsuleOralPar Health USA, LLC49884-14649884-0146-01
penicillaminePenicillamine 250 mg/1Tablet, Film coatedOralPar Health USA, LLC0254-200000254-2000-01
PenicillaminePenicillamine 250 mg/1CapsuleOralActavis Pharma, Inc.0591-417100591-4171-01

Other NDCs under ANDA 211735

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

FDA NDC Directory listings under ANDA 211735
ProductStrengthForm · routeLabelerProduct NDC
PenicillaminePenicillamine 250 mg/1CapsuleOralProficient Rx LP71205-916

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