benzonatate
- Product NDC
- 70518-0043
- 11-digit product format
- 705180043
- Labeler code
- 70518
- Product ID
- 70518-0043_81ab6920-fea4-df94-e053-2a91aa0a2eb7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040749
- Marketing category
- ANDA
- Marketing start
- 2016-12-06
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record