benzonatate
- Product NDC
- 50436-0573
- 11-digit product format
- 504360573
- Labeler code
- 50436
- Product ID
- 50436-0573_7689039e-52e7-4c6e-9125-d898d6a460e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA040627
- Marketing category
- ANDA
- Marketing start
- 2017-03-22
- Marketing end
- 0000-00-00
- Substance
- BENZONATATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-0573-1 | benzonatate | 20 in 1 BOTTLE | CAPSULE | 20 | | 4 |
| 50436-0573-2 | benzonatate | 30 in 1 BOTTLE | CAPSULE | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0573 | BENZONATATE CAPSULE [UNIT DOSE SERVICES] | 4 | Legacy NDC, 2 package rows | 20180929_cf323efe-ae6a-4fb2-a310-9e80b149093b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0573-1 | 50436057301 | 20 in 1 BOTTLE | Historical |
| 50436-0573-2 | 50436057302 | 30 in 1 BOTTLE | Historical |