butalbital, acetaminophen and caffeine

Product NDC
66267-039
11-digit product format
662670039
Labeler code
66267
Product ID
66267-039_715efe3a-d0e5-e425-e053-2a95a90a109a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
butalbital, acetaminophen and caffeine
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA089175
Marketing category
ANDA
Marketing start
1987-01-21
Marketing end
0000-00-00
Substance
BUTALBITAL; ACETAMINOPHEN; CAFFEINE
Active strength
50 mg/1; mg/1; mg/1
Pharmacologic classes
Barbiturates [CS],Barbiturate [EPC],Central Nervous System Stimulant [EPC],Methylxanthine [EPC],Xanthines [CS],Central Nervous System Stimulation [PE]
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 table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66267-039-30EA - Each66267-039e8b9c363-1fbe-4b70-be29-30021d3c6f3812016-10-06
66267-039-60EA - Each66267-0392fa73267-98ad-4723-af74-743bf10f734e12016-10-06
66267-039-90EA - Each66267-0394dac453a-31d8-4baf-ae3e-43df3baa771212016-10-06