Benzonatate

Product NDC: 59762-1122
11-digit product format: 597621122
Labeler code: 59762
Product ID: 59762-1122_4f54d785-c658-48b5-bcd9-bc65a027a62f
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: benzonatate
Dosage form: CAPSULE
Route: ORAL
Labeler: Greenstone LLC
Application: NDA011210
Marketing category: NDA AUTHORIZED GENERIC
Marketing start: 2020-01-06
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: 2023-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
59762-1122-1	2023-12-20	C162847	48780-1	0191ceaa-71b2-198a-e063-dbdaa90aec3e	f84116ad-b924-46a7-9745-d6f14768ac3f
59762-1122-1	2023-07-28	C162847	48780-1	0191ceaa-71b2-198a-e063-dbdaa90aec3e	f84116ad-b924-46a7-9745-d6f14768ac3f

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
59762-1122-1	EA - Each	59762-1122	a7560308-234d-475c-a865-5597f71a0a91	1	2020-02-13

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5P4DHS6ENR	BENZONATATE	104-31-4	BENZONATATE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59762-1122-1	59762112201	100 CAPSULE in 1 BOTTLE (59762-1122-1)	100 capsule	2020-01-06	0000-00-00	No	No	Current