Prescription drug · ANDA
Doxepin (Doxepin hydrochloride) NDC 71335-3177
Doxepin hydrochloride 6 mg/1 · Tablet · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-3177-1 | 71335317701 | 100 TABLET in 1 BOTTLE (71335-3177-1)Marketed from Sep 24, 2026 |
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)
- Doxepin
- Generic name (nonproprietary)
- doxepin hydrochloride
- Active ingredients
- Doxepin hydrochloride — 6 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Bryant Ranch PrepackNDC labeler code 71335
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 202510
- Marketing start
- Listing expires
- Identifiers
- Product ID 71335-3177_87264c52-4386-43d6-88cb-0275236ba97aSPL ID 87264c52-4386-43d6-88cb-0275236ba97a
- Pharmacologic class
- Tricyclic Antidepressant
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
N471335317701followed by a unit qualifier and the quantityPackage 71335-3177-01. 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 71335-3177
- What is NDC 71335-3177?
- 71335-3177 is the product NDC for Doxepin (doxepin hydrochloride), Doxepin hydrochloride 6 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Doxepin (Doxepin hydrochloride).
- What is the active ingredient?
- Doxepin hydrochloride.
- Who is the labeler?
- Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Doxepin?
- 23 other product NDCs are listed under this name. See all Doxepin NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Doxepin products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Doxepin | Doxepin hydrochloride 3 mg/1 | TabletOral | NorthStar Rx LLC | 72603-919 | 72603-0919-01 |
| Doxepin | Doxepin hydrochloride 6 mg/1 | TabletOral | NorthStar Rx LLC | 72603-920 | 72603-0920-01 |
| Doxepin | Doxepin hydrochloride 3 mg/1 | TabletOral | Aurobindo Pharma Limited | 59651-844 | 59651-0844-30 |
| Doxepin | Doxepin hydrochloride 6 mg/1 | TabletOral | Aurobindo Pharma Limited | 59651-845 | 59651-0845-30 |
| Doxepindoxepin hydrochloride | Doxepin hydrochloride 6 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4327 | 70518-4327-00 |
| Doxepin | Doxepin hydrochloride 3 mg/1 | TabletOral | Ajanta Pharma USA Inc. | 27241-280 | 27241-0280-30 |
| Doxepin | Doxepin hydrochloride 6 mg/1 | TabletOral | Ajanta Pharma USA Inc. | 27241-281 | 27241-0281-30 |
| doxepin | Doxepin hydrochloride 3 mg/1 | TabletOral | Zydus Lifesciences Limited | 70771-1528 | 70771-1528-0070771-1528-0170771-1528-03+3 more |
| doxepin | Doxepin hydrochloride 6 mg/1 | TabletOral | Zydus Lifesciences Limited | 70771-1529 | 70771-1529-0070771-1529-0170771-1529-03+3 more |
| doxepin | Doxepin hydrochloride 3 mg/1 | TabletOral | Viona Pharmaceuticals Inc | 72578-181 | 72578-0181-0172578-0181-0572578-0181-06+3 more |
Other NDCs under ANDA 202510
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 |
|---|---|---|---|---|
| Doxepindoxepin hydrochloride | Doxepin hydrochloride 3 mg/1 | TabletOral | Strides Pharma Science Limited | 64380-203 |
| Doxepindoxepin hydrochloride | Doxepin hydrochloride 6 mg/1 | TabletOral | Strides Pharma Science Limited | 64380-204 |
| Doxepindoxepin hydrochloride | Doxepin hydrochloride 6 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4327 |
| Doxepindoxepin hydrochloride | Doxepin hydrochloride 3 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-2474 |
| Doxepindoxepin hydrochloride | Doxepin hydrochloride 6 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-2475 |