Prescription drug · ANDA
benzonatate NDC 71335-0725
Benzonatate 200 mg/1 · Capsule · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-0725-0 | 71335072500 | 6 CAPSULE in 1 BOTTLE (71335-0725-0)Marketed from May 28, 2026 | |
| 71335-0725-1 | 71335072501 | 30 CAPSULE in 1 BOTTLE (71335-0725-1)Marketed from May 28, 2026 | |
| 71335-0725-2 | 71335072502 | 100 CAPSULE in 1 BOTTLE (71335-0725-2)Marketed from May 28, 2026 | |
| 71335-0725-3 | 71335072503 | 45 CAPSULE in 1 BOTTLE (71335-0725-3)Marketed from May 28, 2026 | |
| 71335-0725-4 | 71335072504 | 20 CAPSULE in 1 BOTTLE (71335-0725-4)Marketed from May 28, 2026 | |
| 71335-0725-5 | 71335072505 | 15 CAPSULE in 1 BOTTLE (71335-0725-5)Marketed from May 28, 2026 | |
| 71335-0725-6 | 71335072506 | 21 CAPSULE in 1 BOTTLE (71335-0725-6)Marketed from May 28, 2026 | |
| 71335-0725-7 | 71335072507 | 60 CAPSULE in 1 BOTTLE (71335-0725-7)Marketed from May 28, 2026 | |
| 71335-0725-8 | 71335072508 | 50 CAPSULE in 1 BOTTLE (71335-0725-8)Marketed from May 28, 2026 | |
| 71335-0725-9 | 71335072509 | 90 CAPSULE in 1 BOTTLE (71335-0725-9)Marketed from May 28, 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)
- benzonatate
- Generic name (nonproprietary)
- benzonatate
- Active ingredients
- Benzonatate — 200 mg/1
- Dosage form
- Capsule
- Route
- Oral
- Labeler
- Bryant Ranch Prepack
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 040749
- Marketing start
- Listing expires
- Other FDA classes
- Decreased Tracheobronchial Stretch Receptor Activity (Physiologic effect)
- Identifiers
- Product ID 71335-0725_7db8b947-2c4f-4ca8-867a-bebe58f2327bSPL ID 7db8b947-2c4f-4ca8-867a-bebe58f2327bSPL set ID a788cb01-6dc3-4f28-aaa0-c23ac058c39aRxCUI 197397, 283417UNII 5P4DHS6ENR
- Pharmacologic class
- Non-narcotic Antitussive
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
N471335072500followed by a unit qualifier and the quantityPackage 71335-0725-00. 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 Benzonatate USP is indicated for the symptomatic relief of cough.
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 040749
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 |
|---|---|---|---|---|
| benzonatate | Benzonatate 200 mg/1 | CapsuleOral | Proficient Rx LP | 71205-037 |
| benzonatate | Benzonatate 200 mg/1 | CapsuleOral | Proficient Rx LP | 71205-972 |