benzonatate
- Product NDC
- 55289-175
- 11-digit product format
- 552890175
- Labeler code
- 55289
- Product ID
- 55289-175_29b547bf-c095-14c2-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA040627
- Marketing category
- ANDA
- Marketing start
- 2007-07-25
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55289-175-01 | EA - Each | 55289-175 | d9b21f69-ca8a-457e-824a-187eb39a748a | 1 | 2016-03-04 |
| 55289-175-10 | EA - Each | 55289-175 | ce8992c1-8a0b-4a9f-9638-896409a2962b | 1 | 2012-07-24 |
| 55289-175-12 | EA - Each | 55289-175 | da2d13f5-8633-4496-844a-c3c25301898d | 1 | 2012-07-24 |
| 55289-175-15 | EA - Each | 55289-175 | a3ab1cac-2cb7-43be-a584-fb23b790e836 | 1 | 2012-07-24 |
| 55289-175-20 | EA - Each | 55289-175 | 14af090a-d441-42aa-987e-caef805e3add | 1 | 2012-07-24 |
| 55289-175-21 | EA - Each | 55289-175 | c7c72b6c-67a9-48d4-928a-38ef9ebcc6b3 | 1 | 2012-07-24 |
| 55289-175-30 | EA - Each | 55289-175 | 48789623-6f48-481c-b2a1-8a30ddaf097b | 1 | 2012-07-24 |