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BUTALBITAL AND ACETAMINOPHEN
BUTALBITAL AND ACETAMINOPHEN - 42549-495-30 - (BUTALBITAL AND ACETAMINOPHEN)
Drug Information of BUTALBITAL AND ACETAMINOPHEN
| Product NDC: | 42549-495 |
| Proprietary Name: | BUTALBITAL AND ACETAMINOPHEN |
| Non Proprietary Name: | BUTALBITAL AND ACETAMINOPHEN |
| Active Ingredient(s): | 650; 50 mg/1; mg/1 & nbsp; BUTALBITAL AND ACETAMINOPHEN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BUTALBITAL AND ACETAMINOPHEN
| Product NDC: | 42549-495 |
| Labeler Name: | STAT Rx USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089988 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19941201 |
Package Information of BUTALBITAL AND ACETAMINOPHEN
| Package NDC: | 42549-495-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (42549-495-30) |
NDC Information of BUTALBITAL AND ACETAMINOPHEN
| NDC Code | 42549-495-30 |
| Proprietary Name | BUTALBITAL AND ACETAMINOPHEN |
| Package Description | 30 TABLET in 1 BOTTLE (42549-495-30) |
| Product NDC | 42549-495 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | BUTALBITAL AND ACETAMINOPHEN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19941201 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT Rx USA LLC |
| Substance Name | ACETAMINOPHEN; BUTALBITAL |
| Strength Number | 650; 50 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Barbiturate [EPC],Barbiturates [Chemical/Ingredient] |
