Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 10702-192

Product Visual Gallery

This gallery contains 27 technical images submitted to the FDA as part of the official labeling for Hydrocodone Bitartrate And Acetaminophen (NDC 10702-192). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kvk-tech, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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01 Chemical Structure Hbt

Chemical structure of Hydrocodone Bitartrate and Acetaminophen showing molecular formulas and molecular weight (494.49). The diagram includes atomic bonds and molecular groups for both active ingredients along with associated water molecules (2.5 H2O).*

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02 Chemical Structure Apap

Chemical structure diagram showing the molecular formula C8H9NO2 and molecular weight 151.16, representing the active ingredient in the product Hydrocodone Bitartrate and Acetaminophen.*

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03 Company Logo

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04 Container Label 5mg 300mg 30s

Label for Hydrocodone Bitartrate and Acetaminophen Tablets USP, 5 mg/300 mg, oral tablets. The label includes dosage information, storage instructions, and tamper-evident warnings. It indicates prescription-only status and a 30 tablet quantity. The labeler is KVK-Tech, Inc.*

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05 Container Label 5mg 300mg 100s

Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 5 mg/300 mg, oral tablets. The label includes dosage information, storage instructions, tamper-evident warnings, and states the product is Rx only. Labeler is KVK-Tech, Inc. The package contains 100 tablets.*

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06 Container Label 5mg 300mg 500s

Label for Hydrocodone Bitartrate and Acetaminophen tablets, USP 5 mg / 300 mg by KVK-Tech, Inc. The label details that each tablet contains 5 mg hydrocodone bitartrate and 300 mg acetaminophen. It includes dosing instructions, pharmacist dispensing notes, storage conditions, warning to keep out of reach of children, and tamper-evidence information. The package size is 500 tablets. A barcode and NDC 10702-192-50 are displayed.*

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07 Container Label 5mg 300mg 1000s

Label for Hydrocodone Bitartrate and Acetaminophen Tablets USP, 5 mg/300 mg, supplied by KVK-Tech, Inc. The label includes active ingredient strengths, usage instructions indicating usual adult dosage, storage conditions, a tamper-evident notice, and a barcode with NDC 10702-192-10. The container holds 1000 tablets with prescription-only labeling.*

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08 Container Label 7pt5mg 300mg 30s

Label for Hydrocodone Bitartrate and Acetaminophen Tablets USP 7.5 mg/300 mg, manufactured by KVK-Tech, Inc. The label states that each tablet contains 7.5 mg of hydrocodone bitartrate and 300 mg of acetaminophen. It includes usage instructions, storage conditions, warnings, and packaging details for a bottle of 30 tablets.*

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09 Container Label 7pt5mg 300mg 100s

Label for Hydrocodone Bitartrate and Acetaminophen Tablets, 7.5 mg / 300 mg, oral tablet form. The label includes dosage information and instructions for safe dispensing, labeled for prescription use only, from KVK-Tech, Inc. It specifies storage temperature and packaging in a child-resistant container, with a package size of 100 tablets. The label also includes an NDC number and barcode.*

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10 Container Label 7pt5mg 300mg 500s

Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP, containing 7.5 mg of Hydrocodone Bitartrate and 300 mg of Acetaminophen per tablet. The label directs to dispense the accompanying medication guide, marks the product as prescription only, and specifies package size of 500 tablets. Labeler is KVK-Tech, Inc. Dosage instructions, storage conditions, warnings, and tamper-evident information are printed on the label.*

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11 Container Label 7pt5mg 300mg 1000s

Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5 mg/300 mg in a tablet form. The label is from KVK-Tech, Inc. and indicates a package size of 1000 tablets. It includes dosing instructions, storage conditions, and warnings including child-resistant packaging and tamper evidence information.*

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12 Container Label 10mg 300mg 30s

Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/300 mg oral tablets by KVK-Tech, Inc. The label indicates a 30 tablet bottle with usage and storage instructions, warnings, and pharmacist dispensing guidelines. The NDC code 10702-194-03 is visible along with a barcode.*

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13 Container Label 10mg 300mg 100s

Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/300 mg bottle label by KVK-Tech, Inc. The label states the strength as 10 mg hydrocodone bitartrate and 300 mg acetaminophen per tablet. It indicates an oral tablet dosage form in a 100 tablet container, with storage instructions, tamper evidence notice, and dispensing instructions. The label also includes the NDC 10702-194-01 and the manufacturer's location in Newtown, PA.*

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14 Container Label 10mg 300mg 500s

Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP, with a strength of 10 mg hydrocodone bitartrate and 300 mg acetaminophen per tablet. The label includes dosage instructions, storage conditions, warnings, and a barcode. It notes the product is prescription only, dispensed by KVK-Tech, Inc., and packaged as 500 tablets.*

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15 Container Label 10mg 300mg 1000s

Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 10 mg/300 mg oral tablets, packaged in a bottle of 1000 tablets. Label includes directions for adult dosage, storage instructions, warnings, and pharmacist dispensing information. Manufactured by KVK-Tech, Inc. Contains NDC 10702-194-10.*

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16 Container Label 5mg 325mg 30s

Label for Hydrocodone Bitartrate and Acetaminophen Tablets USP, 5 mg/325 mg, oral tablet dosage form. The label includes dosing information, storage instructions, and a warning about child safety. It is manufactured by KVK-Tech Inc., and the package contains 30 tablets. The NDC visible is 10702-189-03.*

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17 Container Label 5mg 325mg 100s

Label for Hydrocodone Bitartrate and Acetaminophen tablets USP, 5 mg/325 mg, oral tablet form. The label specifies dispensing instructions, dosage guidelines, storage conditions, and tamper evidence. It includes the NDC 10702-189-01, manufacturer KVK-Tech, Inc., and indicates a package size of 100 tablets. The label contains warnings about proper storage and usage.*

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18 Container Label 5mg 325mg 500s

Hydrocodone Bitartrate and Acetaminophen Tablets USP, 5 mg / 325 mg, oral tablets in a 500-count package. The label includes dosage guidelines, storage instructions, a tamper-evident warning, and a barcode. Manufactured by KVK-Tech, Inc., with prescription-only status.*

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19 Container Label 5mg 325mg 1000s

Hydrocodone Bitartrate and Acetaminophen Tablets USP label showing strength 5 mg/325 mg. The label includes dosing instructions, storage conditions, warnings, and pharmacist dispensing guidance. It is for oral tablets, packaged by KVK-Tech, Inc., with a package size of 1000 tablets. The NDC number 10702-189-10 and barcode are also visible.*

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20 Container Label 7pt5mg 325mg 30s

Label for Hydrocodone Bitartrate and Acetaminophen tablets, USP with a strength of 7.5 mg hydrocodone bitartrate and 325 mg acetaminophen per tablet. It is an oral tablet prescription drug by KVK-Tech, Inc., presented in a 30 tablet package. The label includes dosage instructions, storage information, tamper warnings, and a barcode.*

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21 Container Label 7pt5mg 325mg 100s

Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5 mg/325 mg by KVK-Tech, Inc. The label states the dosage strength, ordering information (NDC 10702-190-01), and dispensing instructions. It includes warnings about storage (20° to 25°C), tamper evidence, and keeping the medication out of children's reach. The package contains 100 tablets for oral use, Rx only.*

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22 Container Label 7pt5mg 325mg 500s

Label for Hydrocodone Bitartrate and Acetaminophen Tablets USP, 7.5 mg/325 mg, oral tablets by KVK-Tech, Inc. The label includes NDC 10702-190-50 and indicates a 500 tablet bottle. It provides dosage information, storage instructions, warnings, and pharmacist dispensing guidance.*

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23 Container Label 7pt5mg 325mg 1000s

Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5 mg/325 mg oral tablets in a 1000-count package. The label includes dosing instructions, storage conditions, tamper-evident information, and the labeler KVK-Tech, Inc. The package is marked Rx Only and features a child-resistant closure warning.*

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24 Container Label 10mg 325mg 30s

Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg / 325 mg by KVK-Tech, Inc. The oral tablet package contains 30 tablets and provides dosage and storage information. The label includes a barcode, the NDC number 10702-191-03, and safety warnings about child-resistant containers and tamper evidence.*

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25 Container Label 10mg 325mg 100s

Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325 mg, displayed with dosing information and packaging details. The label shows a quantity of 100 tablets, is marked Rx only, and includes directions to dispense the medication guide. Manufactured by KVK-Tech, Inc., Newtown, PA, USA, with storage and tamper warnings and a barcode.*

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26 Container Label 10mg 325mg 500s

Label for Hydrocodone Bitartrate and Acetaminophen Tablets USP, containing 10 mg hydrocodone bitartrate and 325 mg acetaminophen per tablet. The label includes NDC 10702-191-50 and indicates a package size of 500 tablets. Manufactured by KVK-Tech, Inc., it advises dispensing the accompanying Medication Guide and notes tamper-evident foil under cap.*

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27 Container Label 10mg 325mg 1000s

Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325 mg label displaying dosage strength with directions to dispense accompanying Medication Guide. The label includes dosage instructions, pharmacist instructions for storage and child-resistant packaging, tamper evidence information, quantity of 1000 tablets, and KVK-Tech, Inc. as the manufacturer.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.