Prescription drug · ANDA
Pilocarpine Hydrochloride NDC 59651-225
Pilocarpine hydrochloride 7.5 mg/1 · Tablet, Film coated · Oral · Aurobindo Pharma Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 59651-225-01 | 5965102250159651022501 | 100 TABLET, FILM COATED in 1 BOTTLE (59651-225-01)Marketed from Aug 13, 2019 |
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)
- Pilocarpine Hydrochloride
- Generic name (nonproprietary)
- pilocarpine hydrochloride
- Active ingredients
- Pilocarpine hydrochloride — 7.5 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Aurobindo Pharma LimitedNDC labeler code 59651
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 212377
- Marketing start
- Listing expires
- Other FDA classes
- Cholinergic Agonists (Mechanism)Cholinergic Muscarinic Agonists (Mechanism)
- Identifiers
- Product ID 59651-225_43f023b3-346b-4b93-95b9-ded7f37da9beSPL ID 43f023b3-346b-4b93-95b9-ded7f37da9beSPL set ID 438cfaa3-b5f6-4d75-ac22-b0b4e07bb118RxCUI 1000913, 1001004UNII 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
N459651022501followed by a unit qualifier and the quantityPackage 59651-0225-01. 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 .
Indications (excerpt from the label)
INDICATIONS AND USAGE Pilocarpine hydrochloride tablets are indicated for 1) the treatment of symptoms of dry mouth from salivary gland hypofunction caused by radiotherapy for cancer of the head and neck; and 2) the treatment of symptoms of dry mouth in patients with Sjogren's Syndrome.
Excerpt only. Read the full label for complete information.
About NDC 59651-225
- What is NDC 59651-225?
- 59651-225 is the product NDC for Pilocarpine Hydrochloride, Pilocarpine hydrochloride 7.5 mg/1 tablet, film coated, listed with the FDA by Aurobindo Pharma Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Pilocarpine Hydrochloride.
- What is the active ingredient?
- Pilocarpine hydrochloride.
- Who is the labeler?
- Aurobindo Pharma Limited, NDC labeler code 59651. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Pilocarpine Hydrochloride?
- 21 other product NDCs are listed under this name. See all Pilocarpine Hydrochloride NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Pilocarpine Hydrochloride products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Pilocarpine Hydrochloride | Pilocarpine hydrochloride 5 mg/1 | Tablet, Film coatedOral | AMICI PHARMACEUTICALS LLC | 69292-265 | 69292-0265-01 |
| Pilocarpine Hydrochloride | Pilocarpine hydrochloride 5 mg/1 | Tablet, Film coatedOral | AvPAK | 50268-652 | 50268-0652-12 |
| Pilocarpine Hydrochloride | Pilocarpine hydrochloride 10 mg/mL | Solution/ dropsOphthalmic | Amneal Pharmaceuticals NY LLC | 69238-1745 | 69238-1745-08 |
| Pilocarpine Hydrochloride | Pilocarpine hydrochloride 20 mg/mL | Solution/ dropsOphthalmic | Amneal Pharmaceuticals NY LLC | 69238-1746 | 69238-1746-08 |
| Pilocarpine Hydrochloride | Pilocarpine hydrochloride 40 mg/mL | Solution/ dropsOphthalmic | Amneal Pharmaceuticals NY LLC | 69238-1747 | 69238-1747-08 |
| Pilocarpine Hydrochloridepilocarpine hydrochloride ophthalmic solution | Pilocarpine hydrochloride 10 mg/mL | Solution/ dropsOphthalmic | Somerset Therapeutics, LLC | 70069-181 | 70069-0181-01 |
| Pilocarpine Hydrochloridepilocarpine hydrochloride ophthalmic solution | Pilocarpine hydrochloride 20 mg/mL | Solution/ dropsOphthalmic | Somerset Therapeutics, LLC | 70069-191 | 70069-0191-01 |
| Pilocarpine Hydrochloridepilocarpine hydrochloride ophthalmic solution | Pilocarpine hydrochloride 40 mg/mL | Solution/ dropsOphthalmic | Somerset Therapeutics, LLC | 70069-201 | 70069-0201-01 |
| Pilocarpine Hydrochloride | Pilocarpine hydrochloride 5 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-224 | 59651-0224-01 |
| Pilocarpine hydrochloride | Pilocarpine hydrochloride 5 mg/1 | Tablet, Film coatedOral | American Health Packaging | 68084-928 | 68084-0928-25 |
Other NDCs under ANDA 212377
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Pilocarpine Hydrochloride | Pilocarpine hydrochloride 5 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-224 |