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
70010-907-0170010090701100 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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211735
Marketing start
Listing expires
Identifiers
Product ID 70010-907_2ff8270b-b31e-5b72-e063-6294a90acf7cSPL ID 2ff8270b-b31e-5b72-e063-6294a90acf7cSPL set ID f658b20a-269f-4e78-a79b-a56a5ed8dc1bRxCUI 198070UNII GNN1DV99GXUPC 0370010907010
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

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS Penicillamine capsules are indicated in the treatment of Wilson's disease, cystinuria, and in patients with severe, active rheumatoid arthritis who have failed to respond to an adequate trial of conventional therapy. Available evidence suggests that penicillamine capsules are not of value in ankylosing spondylitis. Wilson’s Disease - Wilson’s disease (hepatolenticular degeneration) occurs in individuals who have inherited an autosomal recessive defect that leads to an accumulation of copper far in excess of metabolic requirements. The excess copper is deposited in several organs and tissues, and eventually produces pathological effects primarily in the liver, where damage progres…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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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