Angina Drops 2083 (angina drops) NDC 63083-2083

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2083Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2083Add 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
63083-2083-2	63083208302	59 mL in 1 BOTTLE, DROPPER (63083-2083-2)Marketed from Aug 15, 1985

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): Angina Drops 2083Suffix: 2083
Generic name (nonproprietary): angina drops
Active ingredients: Hawthorn leaf with flower — 2 [hp_X]/59mLSelenicereus grandiflorus stem — 3 [hp_X]/59mLKalmia latifolia leaf — 3 [hp_X]/59mLPhosphorus — 5 [hp_X]/59mLArsenic trioxide — 6 [hp_X]/59mLDigitalis — 6 [hp_X]/59mLNitroglycerin — 6 [hp_X]/59mLDrimia maritima bulb — 6 [hp_X]/59mLGelsemium sempervirens root — 6 [hp_X]/59mLSpigelia marilandica root — 6 [hp_X]/59mLPotassium carbonate — 12 [hp_X]/59mLArnica montana whole — 30 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Nitrates (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 63083-2083_b4cee559-3d7f-4b9b-b0f1-f1f218046d57SPL ID b4cee559-3d7f-4b9b-b0f1-f1f218046d57SPL set ID 99516597-9f59-4123-bd35-a4a73dd54d2dUNII 6OM09RPY36, 7114SV0MYK, 79N6542N18, 27YLU75U4W, S7V92P67HO, F1T8QT9U8B, G59M7S0WS3, 3629601H5D, 639KR60Q1Q, 467D26HS0B, BQN1B9B9HA, O80TY208ZW
Pharmacologic class: Nitrate Vasodilator

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

N463083208302 followed by a unit qualifier and the quantity

Package 63083-2083-02. 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 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of muscle cramps or spasms, muscular debility, mild abdominal, back or chest pain, or anxiousness.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)