benzonatate
- Product NDC
- 68071-4258
- 11-digit product format
- 680714258
- Labeler code
- 68071
- Product ID
- 68071-4258_bb789b4d-e783-b42d-e053-2a95a90ac965
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040749
- Marketing category
- ANDA
- Marketing start
- 2017-03-22
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 68071-4258 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 68071-4258 | 68071-4258-2 | D | Discontinued by firm | 2026-07-31 | |
| excluded package | package | 68071-4258 | 68071-4258-3 | D | Discontinued by firm | 2026-07-31 | |
| excluded package | package | 68071-4258 | 68071-4258-6 | D | Discontinued by firm | 2026-07-31 |
openFDA label cross-check#
Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| benzonatate | BENZONATATE | Bryant Ranch Prepack | a788cb01-6dc3-4f28-aaa0-c23ac058c39a | 2026-05-28 | Warnings, Adverse reactions | 040749 ANDA040749 |
| benzonatate | BENZONATATE | Proficient Rx LP | 9566b9b9-54ef-423c-8ce4-0f1714052158 | 2022-05-01 | Warnings, Adverse reactions | 040749 ANDA040749 |
| benzonatate | BENZONATATE | Proficient Rx LP | 27156dad-64d6-4ea4-a3da-29e8e096fb01 | 2020-01-01 | Warnings, Adverse reactions | 040749 ANDA040749 |
FDA-Initiated Inactive NDC Indexing#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 68071-4258-2 | 68071425802 | 20 CAPSULE in 1 BOTTLE (68071-4258-2) | 20 capsule | 2018-01-29 | 0000-00-00 | No | No | Current |
| 68071-4258-3 | 68071425803 | 30 CAPSULE in 1 BOTTLE (68071-4258-3) | 30 capsule | 2018-01-29 | 0000-00-00 | No | No | Current |
| 68071-4258-6 | 68071425806 | 60 CAPSULE in 1 BOTTLE (68071-4258-6) | 60 capsule | 2018-01-29 | 0000-00-00 | No | No | Current |