Prescription drug · ANDA
fluoxetine hydrochloride NDC 63629-2200
Fluoxetine hydrochloride 20 mg/1 · Tablet, Coated · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63629-2200-1 | 63629220001 | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (63629-2200-1)Marketed from Aug 22, 2016 |
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)
- fluoxetine hydrochloride
- Generic name (nonproprietary)
- fluoxetine hydrochloride
- Active ingredients
- Fluoxetine hydrochloride — 20 mg/1
- Dosage form
- Tablet, Coated
- Route
- Oral
- Labeler
- Bryant Ranch Prepack
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 203836
- Marketing start
- Listing expires
- Other FDA classes
- Serotonin Uptake Inhibitors (Mechanism)
- Identifiers
- Product ID 63629-2200_f4e092c7-e8de-44b1-957c-b807f4088816SPL ID f4e092c7-e8de-44b1-957c-b807f4088816SPL set ID 72e391aa-1a46-4589-8550-f83ac9241cf1RxCUI 248642UNII I9W7N6B1KJ
- Pharmacologic class
- Serotonin Reuptake Inhibitor
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
N463629220001followed by a unit qualifier and the quantityPackage 63629-2200-01. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 203836
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 |
|---|---|---|---|---|
| fluoxetine hydrochloride | Fluoxetine hydrochloride 10 mg/1 | Tablet, CoatedOral | Bryant Ranch Prepack | 63629-2197 |
| fluoxetine hydrochloride | Fluoxetine hydrochloride 10 mg/1 | Tablet, CoatedOral | Bryant Ranch Prepack | 63629-2198 |
| fluoxetine hydrochloride | Fluoxetine hydrochloride 10 mg/1 | Tablet, CoatedOral | Par Health USA, LLC | 49884-335 |
| fluoxetine hydrochloride | Fluoxetine hydrochloride 20 mg/1 | Tablet, CoatedOral | Par Health USA, LLC | 49884-336 |
| fluoxetine hydrochloride | Fluoxetine hydrochloride 10 mg/1 | Tablet, CoatedOral | Bryant Ranch Prepack | 63629-8989 |
| fluoxetine hydrochloride | Fluoxetine hydrochloride 20 mg/1 | Tablet, CoatedOral | Bryant Ranch Prepack | 63629-8990 |
| fluoxetine hydrochloride | Fluoxetine hydrochloride 10 mg/1 | Tablet, CoatedOral | Bryant Ranch Prepack | 72162-1494 |
| fluoxetine hydrochloride | Fluoxetine hydrochloride 20 mg/1 | Tablet, CoatedOral | Bryant Ranch Prepack | 72162-1495 |