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NDC 71335-0194-04 Butalbital, Acetaminophen, Caffeine and Codeine Phosphate 325; 50; 40; 30 mg/1; mg/1; mg/1; mg/1 Details
Butalbital, Acetaminophen, Caffeine and Codeine Phosphate 325; 50; 40; 30 mg/1; mg/1; mg/1; mg/1
Butalbital, Acetaminophen, Caffeine and Codeine Phosphate is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE.
MedlinePlus Drug Summary
This combination of drugs is used to relieve tension headaches. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
Related Packages: 71335-0194-04Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Acetaminophen, Butalbital, and Caffeine
Product Information
NDC | 71335-0194 |
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Product ID | 71335-0194_05725e50-34b6-49d4-8022-cb204fcf8978 |
Associated GPIs | 65991004100115 |
GCN Sequence Number | 004149 |
GCN Sequence Number Description | butalbit/acetamin/caff/codeine CAPSULE 50-325-30 ORAL |
HIC3 | H3M |
HIC3 Description | OPIOID,NON-SALICYL.ANALGESIC,BARBITURATE,XANTHINE |
GCN | 70140 |
HICL Sequence Number | 001713 |
HICL Sequence Number Description | BUTALBITAL/ACETAMINOPHEN/CAFFEINE/CODEINE PHOSPHATE |
Brand/Generic | Generic |
Proprietary Name | Butalbital, Acetaminophen, Caffeine and Codeine Phosphate |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Butalbital, Acetaminophen, Caffeine and Codeine Phosphate |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | CAPSULE |
Route | ORAL |
Active Ingredient Strength | 325; 50; 40; 30 |
Active Ingredient Units | mg/1; mg/1; mg/1; mg/1 |
Substance Name | ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE |
Labeler Name | Bryant Ranch Prepack |
Pharmaceutical Class | Barbiturate [EPC], Barbiturates [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Full Opioid Agonists [MoA], Methylxanthine [EPC], Opioid Agonist [EPC], Xanthines [CS] |
DEA Schedule | CIII |
Marketing Category | ANDA |
Application Number | ANDA076560 |
Listing Certified Through | 2024-12-31 |
Package
NDC 71335-0194-04 (71335019404)
NDC Package Code | 71335-0194-4 |
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Billing NDC | 71335019404 |
Package | 60 CAPSULE in 1 BOTTLE (71335-0194-4) |
Marketing Start Date | 2021-12-13 |
NDC Exclude Flag | N |
Pricing Information | N/A |