Vtol LQ

Product NDC: 70154-111
11-digit product format: 701540111
Labeler code: 70154
Product ID: 70154-111_ed1e4388-d290-ff7d-e053-2a95a90a61ca
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: butalbital, acetaminophen and caffeine
Dosage form: SYRUP
Route: ORAL
Labeler: Monarch PCM, LLC
Application: ANDA040387
Marketing category: ANDA
Marketing start: 2019-11-11
Marketing end: 2023-11-10
Substance: ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Active strength: 325 mg/15mL; mg/15mL; mg/15mL
Pharmacologic classes: Barbiturate [EPC], Barbiturates [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS]
DEA schedule: CIII
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
70154-111-16	ML - Milliliter	70154-111	291d20e7-101e-4f8e-a5e0-96bdc7ebf414	1	2020-03-10

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
362O9ITL9D	ACETAMINOPHEN	103-90-2	ACETAMINOPHEN
KHS0AZ4JVK	BUTALBITAL	77-26-9	BUTALBITAL
3G6A5W338E	CAFFEINE	58-08-2	CAFFEINE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70154-111-16	70154011116	473 mL in 1 BOTTLE, PLASTIC (70154-111-16)	473 ml	2019-11-11	0000-00-00	No	No	Current