Benzonatate
- Product NDC
- 71205-643
- 11-digit product format
- 712050643
- Labeler code
- 71205
- Product ID
- 71205-643_6bfa0eeb-17e2-4b47-a91b-546d67af50d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA206948
- Marketing category
- ANDA
- Marketing start
- 2018-12-21
- Substance
- BENZONATATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Decreased Tracheobronchial Stretch Receptor Activity [PE], Non-narcotic Antitussive [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5P4DHS6ENR | BENZONATATE | 104-31-4 | BENZONATATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-643-10 | 71205064310 | 10 CAPSULE in 1 BOTTLE (71205-643-10) | 10 capsule | 2022-03-10 | No | No | Historical |
| 71205-643-14 | 71205064314 | 14 CAPSULE in 1 BOTTLE (71205-643-14) | 14 capsule | 2022-04-05 | No | No | Historical |
| 71205-643-15 | 71205064315 | 15 CAPSULE in 1 BOTTLE (71205-643-15) | 15 capsule | 2022-03-10 | No | No | Historical |
| 71205-643-20 | 71205064320 | 20 CAPSULE in 1 BOTTLE (71205-643-20) | 20 capsule | 2022-03-10 | No | No | Historical |
| 71205-643-21 | 71205064321 | 21 CAPSULE in 1 BOTTLE (71205-643-21) | 21 capsule | 2022-03-10 | No | No | Historical |
| 71205-643-30 | 71205064330 | 30 CAPSULE in 1 BOTTLE (71205-643-30) | 30 capsule | 2022-03-10 | No | No | Historical |
| 71205-643-60 | 71205064360 | 60 CAPSULE in 1 BOTTLE (71205-643-60) | 60 capsule | 2022-03-10 | No | No | Historical |
| 71205-643-90 | 71205064390 | 90 CAPSULE in 1 BOTTLE (71205-643-90) | 90 capsule | 2022-03-10 | No | No | Historical |